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1,127 catalysts · 18,987 approval · 5,000 device 510k · 4,779 phase readout · 4,728 grant · 2,391 8k filing · 2,000 device pma

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  • approval18,987
  • device 510k5,000
  • phase readout4,779
  • grant4,728
  • 8k filing2,391
  • device pma2,000
device recall
2,000
  • recall1,126
  • device adverse event1,000
  • earnings295
  • therapy area

    no tagged catalysts yet

    Week of Oct 27, 2025

    12
    ›Oct 29, 2025recall268d agoGraviti Pharmaceuticals Private Limited recall (Cls II)Graviti Pharmaceuticals Inc

    Bupropion Hydrochloride Extended-Release Tablets USP (XL), 300 mg, 30-count bottles, Rx Only, Mfd. by: Graviti Pharmaceuticals Private Limited, Sangareddy, Telangana, India, Dist. by: Rising Phar, NDC 16571-863-03. — Reason: Failed Tablet/Capsule Specifications — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 29, 2025recall268d agoLannett Company Inc. recall (Cls II)Lannett Co Inc

    Niacin Extended-release Tablets, USP, 1,000 mg, Rx Only, 90 Tablets per bottle, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136. NDC: 62175-322-46 — Reason: Failed Dissolution Specifications — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 29, 2025recall268d agoThe Harvard Drug Group LLC recall (Cls II)Almatica Pharma LLC

    Gabapentin Capsules, USP, 100 mg, 10 Capsules (10 x 1 blister pack), Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268, USA, NDC 0904-6665-61 (Blister pack), NDC 55154-3363-0 (Outer Bag). — Reason: Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity . — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 29, 2025recall268d agoJB Chemicals and Pharmaceuticals Ltd recall (Cls III)Island Pharmaceuticals Ltd

    Cetirizine Hydrochloride Tablets USP 10 mg, 100 Tablets bottles, Manufactured by: Unique Pharmaceuticals Labs, (A Div. of J.B. Chemicals & Pharmaceuticals, Ltd.), Mumbai 400 030, India. Distributed by: Rising Pharma Holdings, Inc., East Brunswick, NJ 08816, NDC 16571-402-10. — Reason: Tablet/Capsules Imprinted with Wrong ID — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 29, 2025recall268d agoibspot recall (Cls II)

    Taoscare Motion Sickness Patches 36-count box, Henan Xinyongtal Medical Technology., Ltd., Address: he nan sheng zhou kou shi huai yang xian gong ye yuan qu, X003SR097N — Reason: Marketed Without an Approved NDA/ANDA — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 29, 2025recall268d agoUSV Private Limited recall (Cls II)SOLA Pharmaceuticals Inc

    Olopatadine Hydrochloride Ophthalmic Solution USP 0.1 %, 5 mL (0.17 FL OZ) bottles, Manufactured for: SOLA PHARMACEUTICALS LLC, Baton Rouge, LA 70810, NDC 70512-0520-05 — Reason: Failed Impurities/Degradation Specifications: The result for 'Any individual unspecified impurity' exceeds the specification limit. — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 29, 2025recall268d agoMedline Industries, LP recall (Cls II)

    Medline, Alcohol Prep Pads (2-Ply Pad, 70% Isopropyl Alcohol), 100 eaches per box, 10 boxes per case (1,000 eaches per case), Single Use Only, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL, 60093 USA, NDC 55329-811-30. — Reason: Subpotent Drug — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 29, 2025recall268d agoThe Harvard Drug Group LLC recall (Cls II)Almatica Pharma LLC

    Gabapentin Capsules, USP, 100 mg, 100 Capsules (10 x 10 blister packs), Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268, USA, NDC 0904-6665-61 — Reason: Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity . — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 29, 2025recall268d agoJB Chemicals and Pharmaceuticals Ltd recall (Cls III)Island Pharmaceuticals Ltd

    Cetirizine Hydrochloride Tablets USP 10 mg, 500 Tablets bottles, Manufactured by: Unique Pharmaceuticals Labs, (A Div. of J.B. Chemicals & Pharmaceuticals, Ltd.), Mumbai 400 030, India. Distributed by: Rising Pharma Holdings, Inc., East Brunswick, NJ 08816, NDC 16571-402-50 — Reason: Tablet/Capsules Imprinted with Wrong ID — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 29, 2025recall268d agoChurch & Dwight Co., Inc. recall (Cls II)CHURCH & DWIGHT CO INC /DE/

    ZICAM" MEDICATED FRUIT DROPS ELDERBERRY FLAVOR, 25-drops per bottle, Distributed by: Church & Dwight Co., Inc. Ewing, NJ 08628, NDC 10237-469-25 — Reason: Labeling: Label Mix-up: The product in the bottle contains elderberry and the label failed to indicate the inclusion of elderberry as an ingredient. — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 29, 2025recall268d agoAspiro Pharma Limited recall (Cls II)Aspiro Pharma Ltd

    Ketorolac Tromethamine Injection, USP, 60 mg/2 mL (30 mg/mL), 2 mL Single-Dose Vial, For Intramuscular Use Only, Rx only, Mfd. for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, Mfd. by: ASPIRO PHARMA LIMITED, Telangana - 502281, INDIA., U.S. Contact Number: 1-866-495-1995, NDC 31722-307-25 (Carton), 31722-307-02 (Vial label). — Reason: Presence of Particulate Matter: Particulate matter identified as glass — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 29, 2025recall268d agoBristol-Myers Squibb Company recall (Cls II)BRISTOL MYERS SQUIBB CO

    Opdualag (nivolumab and relatlimab-rmbw) injection, 240 mg and 80 mg/20 mL (12mg and 4mg/mL),Single Dose Vial, RX Only, Bristol-Myers Squibb Company, Princeton, NJ 08543, NDC 0003-7125-11 — Reason: Lack of Assurance of Sterility. — Status: Ongoing

    full page →fda recalls ↗

    Week of Nov 3, 2025

    38
    ›Nov 5, 2025recall261d agoProRx LLC recall (Cls II)Novo Nordisk AS

    Semaglutide Injection, 10 mg/4 mL (2.5 mg/mL), 4mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Jeffers Cir, Exton, PA 19341. NDC: 84139-225-04 — Reason: Lack of Assurance of Sterility — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall
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    261d ago
    ProRx LLC recall (Cls II)Novo Nordisk AS

    Semaglutide Injection, 6mg/2.4mL (2.5 mg/mL), 2.4mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Jeffers Cir, Exton, PA 19341. NDC: 84139-225-08 — Reason: Lack of Assurance of Sterility — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoFARMAKEIO OUTSOURCING LLC recall (Cls II)Sun Pharmaceutical Industries Ltd

    Testosterone / Triamcinolone Acetonide 25MG/5MCG, 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0379-01 — Reason: CGMP Deviations: Potential presence of metal particulate matter — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoTeva Pharmaceuticals USA, Inc recall (Cls II)Terns Pharmaceuticals, Inc.

    Prazosin Hydrochloride, Capsules, USP, 2 mg, Rx only, Distributed by TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, a) 100 Capsules, NDC 0093-4068-01, b) 1000 Capsules, NDC 0093-4068-10 — Reason: CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit for the above specified lots. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoProRx LLC recall (Cls II)Novo Nordisk AS

    Semaglutide Injection, 2.5mg/1mL (2.5 mg/mL), 1mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Jeffers Cir, Exton, PA 19341. NDC: 84139-225-06 — Reason: Lack of Assurance of Sterility — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoSUN PHARMACEUTICAL INDUSTRIES INC recall (Cls II)TEVA PHARMACEUTICAL INDUSTRIES LTD

    Lisdexamfetamine Dimesylate Capsules, 60 mg, CII, 100-count bottle, Rx only, Manufactured by: OHM Laboratories, New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 57664-051-88. — Reason: Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 12-month long term stability station (25¿C, 60%RH) for Lisdexamfetamine dimesylate capsules. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoTeva Pharmaceuticals USA, Inc recall (Cls II)Terns Pharmaceuticals, Inc.

    Prazosin Hydrochloride, Capsules, USP, 1 mg, Rx only, Distributed by TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, a) 100 Capsules, NDC 0093-4067-01, b) 1000 Capsules, NDC 0093-4067-10 — Reason: CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit for the above specified lots. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoFARMAKEIO OUTSOURCING LLC recall (Cls II)Transdermal Delivery Solutions Corp

    Testosterone 50MG, 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0387-01 — Reason: CGMP Deviations: Potential presence of metal particulate matter — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoHeritage Pharmaceuticals Inc recall (Cls II)Hepion Pharmaceuticals, Inc.

    Desipramine Hydrochloride Tablets, USP, 25 mg, 100 count bottle (NDC 23155-579-01), Rx only, Manufactured by: USV Private Limited, Daman, India, Manufactured for: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816. — Reason: CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoFARMAKEIO OUTSOURCING LLC recall (Cls II)Transdermal Delivery Solutions Corp

    Testosterone 62.5 MG, 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0383-01 — Reason: CGMP Deviations: Potential presence of metal particulate matter — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoLetco Medical LLC recall (Cls III)QOL Medical LLC

    Espumil, Lipophilic foam base, 500 ml, 24G15-T02-115604 — Reason: Labeling: Not Elsewhere Classified — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoEndo USA, Inc. recall (Cls III)Par Pharmaceutical Inc

    Everolimus tablets 7.5mg, 28 tablets (each carton contains 4 blister strips with 7 tablets each), Rx only, Manufactured by: Par Pharmaceutical Chestnut Ridge, NY 10977 NDC# 49884-127-91 — Reason: Failed Impurities/Degradation Specifications: Out of specification for impurity IP-C. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoProRx LLC recall (Cls II)Novo Nordisk AS

    Semaglutide Injection, 8mg/3.2mL (2.5 mg/mL), 3.2mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Jeffers Cir, Exton, PA 19341. NDC: 84139-225-09 — Reason: Lack of Assurance of Sterility — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoSamsung Bioepis Co., Ltd. recall (Cls II)Samsung Bioepis Co Ltd

    HADLIMA (adalimumab-bwwd) injection, 40mg/0.8 mL, 2 Single-dose Prefilled Syringes per carton, Rx only, Manufactured for: Organon LLC, a subsidiary of ORGANON & Co, Jersey City, NJ 07302, Manufactured by: SAMSUN BIOEPIS Co., Ltd, Incheon, Republic of Korea, NDC 78206-183-01. — Reason: Lack of Assurance of Sterility. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoProRx LLC recall (Cls II)Eli Lilly and Co

    Tirzepatide Injection, 27 mg/3 mL (9 mg/mL), 3mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Jeffers Cir, Exton, PA 19341. NDC: 84139-209-03 — Reason: Lack of Assurance of Sterility — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoFARMAKEIO OUTSOURCING LLC recall (Cls II)Sun Pharmaceutical Industries Ltd

    Testosterone / Triamcinolone Acetonide Pellet (100MG/20MCG), 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0367-01 — Reason: CGMP Deviations: Potential presence of metal particulate matter — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoHeritage Pharmaceuticals Inc recall (Cls II)Hepion Pharmaceuticals, Inc.

    Desipramine Hydrochloride Tablets, USP, 150 mg, 50 count bottle (NDC 23155-583-25), Rx only, Manufactured by: USV Private Limited, Daman, India, Manufactured for: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816. — Reason: CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoKenvue Brands LLC recall (Cls II)JOHNSON & JOHNSON

    TYLENOL, Acetaminophen, Extra Strength, 24 Caplets, 500mg each, distributed by: Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division, Fort Washington, PA 19034, NDC: 50580-378-04. — Reason: Defective Container — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoSUN PHARMACEUTICAL INDUSTRIES INC recall (Cls II)TEVA PHARMACEUTICAL INDUSTRIES LTD

    Lisdexamfetamine Dimesylate Capsules, 50 mg, CII, 100-count bottle, Rx only, Manufactured by: OHM Laboratories, New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 57664-050-88. — Reason: Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 12-month long term stability station (25¿C, 60%RH) for Lisdexamfetamine dimesylate capsules. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoAmerisource Health Services LLC recall (Cls II)Appco Pharma LLC

    Prazosin Hydrochloride, Capsules, USP, 5 mg, 20 capsules (5x4) cartons, Rx only, Distributed by American Health Packaging, Columbus, Ohio 43217, carton NDC 60687-572-32, Individual unit dose: NDC 60687-572-33 — Reason: Failed Impurities/Degradation Specification: presence of N-nitroso Prazosin impurity C above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoProRx LLC recall (Cls II)Novo Nordisk AS

    Semaglutide Injection, 12.5/5mL (2.5 mg/mL), 5mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Jeffers Cir, Exton, PA 19341. NDC: 84139-225-09 — Reason: Lack of Assurance of Sterility — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoFARMAKEIO OUTSOURCING LLC recall (Cls II)Sun Pharmaceutical Industries Ltd

    Testosterone / Triamcinolone Acetonide, 12.5MG/2.5MCG, 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0363-01 — Reason: CGMP Deviations: Potential presence of metal particulate matter — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoEndo USA, Inc. recall (Cls III)Par Pharmaceutical Inc

    Everolimus tablets 2.5 mg, 28 tablets (each carton contains 4 blister strips with 7 tablets each), Rx only, Manufactured by: Par Pharmaceutical Chestnut Ridge, NY 10977 NDC# 49884-119-91 — Reason: Failed Impurities/Degradation Specifications: Out of specification for impurity IP-C. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoFARMAKEIO OUTSOURCING LLC recall (Cls II)Sun Pharmaceutical Industries Ltd

    Testosterone / Triamcinolone Acetonide Pellet (37.5MG/7.5MCG), 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0380-01 — Reason: CGMP Deviations: Potential presence of metal particulate matter — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoProRx LLC recall (Cls II)Novo Nordisk AS

    Semaglutide Injection, 5 mg/2 mL (2.5 mg/mL), 2mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Jeffers Cir, Exton, PA 19341. NDC: 84139-225-02 — Reason: Lack of Assurance of Sterility — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoOtsuka ICU Medical LLC recall (Cls II)Revalesio Corp

    0.9% SODIUM CHLORIDE Injection, USP, 100 mL, Rx only, ICU Medical, Inc., Lake Forest, Illinois, 60045, USA, NDC 0990-7984-37 — Reason: Lack of Assurance of Sterility: Potential for flexible container leaks. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoFARMAKEIO OUTSOURCING LLC recall (Cls II)Transdermal Delivery Solutions Corp

    Testosterone 25MG, 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0389-01 — Reason: CGMP Deviations: Potential presence of metal particulate matter — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoAmerisource Health Services LLC recall (Cls II)Appco Pharma LLC

    Prazosin Hydrochloride, Capsules, USP, 2 mg, 100 capsules (10x10) cartons, Rx only, Distributed by American Health Packaging, Columbus, Ohio 43217, Carton NDC 68084-997-01, Individual unit dose: NDC 68084-997-11 — Reason: Failed Impurities/Degradation Specification: presence of N-nitroso Prazosin impurity C above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoFARMAKEIO OUTSOURCING LLC recall (Cls II)Sun Pharmaceutical Industries Ltd

    Testosterone / Triamcinolone Acetonide Pellet (200MG/40MCG), 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0364-01 — Reason: CGMP Deviations: Potential presence of metal particulate matter — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoFARMAKEIO OUTSOURCING LLC recall (Cls II)Sun Pharmaceutical Industries Ltd

    Testosterone / Triamcinolone Acetonide 87.5MG/17.5MCG, 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0382-01 — Reason: CGMP Deviations: Potential presence of metal particulate matter — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoFARMAKEIO OUTSOURCING LLC recall (Cls II)Transdermal Delivery Solutions Corp

    Testosterone Regular Release 50 MG, 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0401-01 — Reason: CGMP Deviations: Potential presence of metal particulate matter — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoFARMAKEIO OUTSOURCING LLC recall (Cls II)Sun Pharmaceutical Industries Ltd

    Testosterone / Triamcinolone Acetonide 50MG/10MCG, 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0365-01 — Reason: CGMP Deviations: Potential presence of metal particulate matter — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoHeritage Pharmaceuticals Inc recall (Cls II)Hepion Pharmaceuticals, Inc.

    Desipramine Hydrochloride Tablets, USP, 10 mg, 100 - count bottle (NDC 23155-578-01), Rx only, Manufactured by: USV Private Limited, Daman, India, Manufactured for: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816. — Reason: CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoSUN PHARMACEUTICAL INDUSTRIES INC recall (Cls II)TEVA PHARMACEUTICAL INDUSTRIES LTD

    Lisdexamfetamine Dimesylate Capsules, 70 mg, CII, 100-count bottle, Rx only, Manufactured by: OHM Laboratories, New Brunswick, NJ 08901, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 57664-052-88. — Reason: Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 12-month long term stability station (25¿C, 60%RH) for Lisdexamfetamine dimesylate capsules. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoACME UNITED CORPORATION recall (Cls II)ACME UNITED CORP

    Sting Relief Swabs, First Aid Only, 10 Swabs per box, part number 19-001, Manufactured for: Acme United Corporation, 1 Waterview Dr. Shelton, CT, Made in the USA UPC 738743190015 — Reason: Product Mix-up — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoAmerisource Health Services LLC recall (Cls II)Appco Pharma LLC

    Prazosin Hydrochloride, Capsules, USP, 1 mg, 100 capsules (10x10) cartons, Rx only, Distributed by American Health Packaging, Columbus, Ohio 43217, Carton NDC 68084-996-01. Individual unit dose: NDC 68084-996-11 — Reason: Failed Impurities/Degradation Specification: presence of N-nitroso Prazosin impurity C above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit — Status: Ongoing

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    ›Nov 5, 2025recall261d agoFARMAKEIO OUTSOURCING LLC recall (Cls II)Transdermal Delivery Solutions Corp

    Testosterone 200 MG, 1 PELLET (STERILE) FOR SUBCUTANEOUS INSERTION, RX ONLY, FarmaKeio Outsourcing, 920 S Kimball Ave, Ste 100, Southlake, TX 76092. NDC 73693-0381-01 — Reason: CGMP Deviations: Potential presence of metal particulate matter — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 5, 2025recall261d agoHeritage Pharmaceuticals Inc recall (Cls II)Hepion Pharmaceuticals, Inc.

    Desipramine Hydrochloride Tablets, USP, 50 mg, 100 count bottle (NDC 23155-580-01), Rx only, Manufactured by: USV Private Limited, Daman, India, Manufactured for: Avet Pharmaceuticals Inc., East Brunswick, NJ 08816. — Reason: CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level. — Status: Ongoing

    full page →fda recalls ↗
    $ILPLF
    $CHD96.19-0.97%
    $ILPLF
    $BMY61.51+1.23%
    $TEVA31.18+3.42%
    $TERN52.95-0.03%
    $TERN52.95-0.03%
    $HEPA
    $HEPA
    $JNJ259.27+1.42%
    $TEVA31.18+3.42%
    $HEPA
    $ACU45.90-1.54%
    $TEVA31.18+3.42%
    $HEPA