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calendar

28,263 catalysts · 17,815 approval · 4,115 device 510k · 2,475 grant · 1,585 device recall · 1,367 device pma · 906 recall

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  • approval17,815
  • device 510k4,115
  • grant2,475
  • device recall1,585
  • device pma1,367
  • recall906
therapy area

no tagged catalysts yet

Week of Nov 25, 2024

39
›Nov 27, 2024recall645d agoLupin Pharmaceuticals Inc. recall (Cls II)LB PHARMACEUTICALS INC

Ramipril Capsules USP 10 mg, a) 90 count (NDC 68180-591-09), b) 100 count NDC 68180-591-01), and c) 500 count (NDC 68180-591-02) bottles, Rx only, Manufactured for Lupin Pharmaceuticals, Inc., Baltimore, MD, Manufactured by Lupin Limited, Goa, India — Reason: CGMP Deviations: Active pharmaceutical ingredient was sourced from an unapproved vendor — Status: Terminated

full page →fda recalls ↗
›Nov 27, 2024recall645d agoDr. Reddy's Laboratories, Inc. recall (Cls III)DR REDDYS LABORATORIES LTD

IBU (ibuprofen) 600 mg tablets, 500-count bottle, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 55111-683-05 — Reason: Failed Tablet/Capsule Specifications — Status: Ongoing

full page →fda recalls ↗
›Nov 27, 2024recall645d agoThe Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories recall (Cls II)Moberg Pharma AB

Guaifenesin Dextromethorphan Syrup, 100 mg/10mg per 5 mL, Major Pharmaceuticals 8401 Bearing Drive, Suite 100, Indianapolis, IN, 46268, NDC 0904-7134-70 — Reason: Failed Impurity/Degradation Specifications — Status: Terminated

full page →fda recalls ↗
›Nov 27, 2024recall645d agoThe Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories recall (Cls II)Moberg Pharma AB

Guaifenesin Dextromethorphan Syrup, 200 mg/20mg per 10 mL, Major Pharmaceuticals 8401 Bearing Drive, Suite 100, Indianapolis, IN, 46268, NDC 0904-7135-72 — Reason: Failed Impurity/Degradation Specifications — Status: Terminated

full page →fda recalls ↗
›Nov 27, 2024recall645d agoSafecor Health, LLC recall (Cls II)Aspire Biopharma Holdings, Inc.

Aspirin Chewable tablet 81 mg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-129-01 — Reason: cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity. — Status: Ongoing

full page →fda recalls ↗
›Nov 27, 2024recall645d agoSafecor Health, LLC recall (Cls II)

Calcium Carbonate Chewable 500 mg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-106-01 — Reason: cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity. — Status: Ongoing

full page →fda recalls ↗
›Nov 27, 2024recall645d agoTailstorm Health INC recall (Cls II)F. Hoffmann-La Roche Ltd

BEVACIZUMAB (AVASTIN)1.25mg/0.05mL, Sterile Injection, 0.5 mL Single-Dose Syringe, Rx Only, Repackaged by: Medivant Healthcare: 24416 N 19th Ave, Phoenix, AZ, NDC 81483-0041-1 — Reason: Lack of Sterility Assurance — Status: Terminated

full page →fda recalls ↗
›Nov 27, 2024recall645d agoLupin Pharmaceuticals Inc. recall (Cls II)LB PHARMACEUTICALS INC

Ramipril Capsules USP 2.5 mg, a) 90 count (NDC 68180-589-09), b) 100 count NDC 68180-589-01), and c) 500 count (NDC 68180-589-02) bottles, Rx only, Manufactured for Lupin Pharmaceuticals, Inc., Baltimore, MD, Manufactured by Lupin Limited, Goa, India — Reason: CGMP Deviations: Active pharmaceutical ingredient was sourced from an unapproved vendor — Status: Terminated

full page →fda recalls ↗
›Nov 27, 2024recall645d agoLupin Pharmaceuticals Inc. recall (Cls II)LB PHARMACEUTICALS INC

Ramipril Capsules USP 5 mg, a) 90 count (NDC 68180-590-09), b) 100 count NDC 68180-590-01), and c) 500 count (NDC 68180-590-02) bottles, Rx only, Manufactured for Lupin Pharmaceuticals, Inc., Baltimore, MD, Manufactured by Lupin Limited, Goa, India — Reason: CGMP Deviations: Active pharmaceutical ingredient was sourced from an unapproved vendor — Status: Terminated

full page →fda recalls ↗
›Nov 27, 2024recall645d agoSafecor Health, LLC recall (Cls II)

Docusate Sodium 250 mg, 1 Softgel in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-101-01 — Reason: cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity. — Status: Ongoing

full page →fda recalls ↗
›Nov 27, 2024recall645d agoNoven Pharmaceuticals Inc recall (Cls II)NRX Pharmaceuticals, Inc.

Xelstrym (dextroamphetamine) transdermal system, 13.5 mg dextroamphetamine/9 hours, 30 individually sealed transdermal patches, inside a foil-sealed polypropylene tray, packed in a paper carton/box, MANUFACTURED BY NOVEN PHARMACEUTICALS, INC., Miami, FL 33186 United Sates, NDC 68968-0215-3 — Reason: Defective Delivery System: The product does not meet predetermined specifications for Coldflow (adhesive). — Status: Ongoing

full page →fda recalls ↗
›Nov 27, 2024recall645d agoEvaric Pharmaceuticals Inc. recall (Cls II)Oric Pharmaceuticals, Inc.

Lisinopril Tablets, USP 10 mg, 90 tablets per bottle, Rx Only, Distributed by: Walmart, Bentonville, AR 72716, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, Packaged by: Legacy Pharmaceutical Packaging LLC, Earth City, MO 63045, NDC# 68645-610-90. — Reason: Presence of Foreign Object: A pharmacist discovered a metal fragment embedded in a lisinopril 10 mg tablet. — Status: Completed

full page →fda recalls ↗
›Nov 27, 2024recall645d agoSafecor Health, LLC recall (Cls II)

Vitamin B1, 100 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-108-01 — Reason: cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity. — Status: Ongoing

full page →fda recalls ↗
›Nov 27, 2024recall645d agoSafecor Health, LLC recall (Cls II)

Vitamin D3, 25 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-104-01 — Reason: cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity. — Status: Ongoing

full page →fda recalls ↗
›Nov 27, 2024device 510k645d agoNextbiomedical Co., Ltd. — Nexpowder (510k cleared)ACRO BIOMEDICAL CO., LTD.

Product code: QAU. Advisory committee: General, Plastic Surgery. Type: Traditional

full page →fda device 510k ↗
›Nov 27, 2024device 510k645d agoDeka Research & Development Corp. — Remunity System (510k cleared)

Product code: QJY. Advisory committee: General Hospital. Type: Special

full page →fda device 510k ↗
›Nov 27, 2024device 510k645d agoEizo Corporation — RadiForce RX570; RadiForce RX570-AR (510k cleared)

Product code: PGY. Advisory committee: Radiology. Type: Abbreviated

full page →fda device 510k ↗
›Nov 27, 2024device 510k645d agoOntact Health Co., Ltd. — Sonix Health (510k cleared)

Product code: QIH. Advisory committee: Radiology. Type: Traditional

full page →fda device 510k ↗
›Nov 27, 2024device 510k645d agoSamsung Medison Co., Ltd. — HERA W10 Diagnostic Ultrasound System; HERA W9 Diagnostic Ultrasound System (510k cleared)

Product code: IYN. Advisory committee: Radiology. Type: Traditional

full page →fda device 510k ↗
›Nov 27, 2024device 510k645d agoEasymed Instruments Co., Ltd. — Pelvic Floor Stimulator (Intrelief PFE) (510k cleared)

Product code: KPI. Advisory committee: Gastroenterology, Urology. Type: Traditional

full page →fda device 510k ↗
›Nov 27, 2024device 510k645d agoShenzhen Walton Technology Co., Ltd. — LED Light Therapy Machine (G1, G3, G4, G6) (510k cleared)Fortior Technology (Shenzhen) Co., Ltd./ADR

Product code: OHS. Advisory committee: General, Plastic Surgery. Type: Traditional

full page →fda device 510k ↗
›Nov 27, 2024device 510k645d agoCyden Limited — SmoothSkin Pure Switch (SSC1) (510k cleared)

Product code: OHT. Advisory committee: General, Plastic Surgery. Type: Special

full page →fda device 510k ↗
›Nov 27, 2024device 510k645d agoKarl Storz SE & CO. KG — KARL STORZ Pediatric Cysto-Urethro-Fiberscope (11274BCU1) (510k cleared)

Product code: FBO. Advisory committee: Gastroenterology, Urology. Type: Special

full page →fda device 510k ↗
›Nov 27, 2024device 510k645d agoVilex, LLC — TACTIX Vector Syndesmosis System (510k cleared)

Product code: HTN. Advisory committee: Orthopedic. Type: Special

full page →fda device 510k ↗
›Nov 27, 2024device 510k645d agoCeragem Co., Ltd. — Ceragem Automatic Thermal Massager (CGM-MB-1902) (510k cleared)

Product code: JFB. Advisory committee: Physical Medicine. Type: Special

full page →fda device 510k ↗
›Nov 27, 2024device 510k645d agoPrevest Denpro Limited — C&B Ceramic; C&B Permanent; C&B Interim (510k cleared)

Product code: EBF. Advisory committee: Dental. Type: Traditional

full page →fda device 510k ↗
›Nov 27, 2024device 510k645d agoCellmyx — AirSculpt Body Contouring System (AIRS-1-SYS) (510k cleared)

Product code: QPB. Advisory committee: General, Plastic Surgery. Type: Traditional

full page →fda device 510k ↗
›Nov 27, 2024device 510k645d agoSharkninja Operating, LLC — CryoGlow (FW3XXXX) (510k cleared)

Product code: OHS. Advisory committee: General, Plastic Surgery. Type: Traditional

full page →fda device 510k ↗
›Nov 27, 2024device 510k645d agoBard Access Systems, Inc. — PowerLoc™ Max Power Injectable Infusion Set; SafeStep™ Huber Needle Set (510k cleared)

Product code: PTI. Advisory committee: General Hospital. Type: Traditional

full page →fda device 510k ↗
›Nov 27, 2024device 510k645d agoSpectrum Vascular — SV Spectrum MRC Central Venous Catheter; SV Spectrum MR Central Venous Catheter; SV Central Venous Catheter (510k cleared)

Product code: FOZ. Advisory committee: General Hospital. Type: Traditional

full page →fda device 510k ↗
›Nov 27, 2024device 510k645d agoConmed Corporation — BioBrace® (510k cleared)CONMED Corp

Product code: OWW. Advisory committee: General, Plastic Surgery. Type: Traditional

full page →fda device 510k ↗
›Nov 27, 2024device 510k645d agoZhejiang Zhonglei Medical Technology Co. , Ltd. — Power wheelchair (510k cleared)Zhejiang Xinkanghe Biomedical Technology Co Ltd

Product code: ITI. Advisory committee: Physical Medicine. Type: Traditional

full page →fda device 510k ↗
›Nov 29, 2024approval643d agoYESINTEK (USTEKINUMAB-KFCE) — FDA approvalustekinumab biosimilar

Sponsor: BIOCON BIOLOGICS INC. Form: INJECTABLE. Route: INJECTION

full page →ustekinumab biosimilar →fda approvals ↗
›Nov 29, 2024approval643d agoDAYTRANA (METHYLPHENIDATE) — FDA approvalNoven Pharmaceuticals Inc

Sponsor: NOVEN PHARMS INC. Form: FILM, EXTENDED RELEASE. Route: TRANSDERMAL

full page →fda approvals ↗
›Nov 29, 2024approval643d agoXELSTRYM (DEXTROAMPHETAMINE) — FDA approvalNoven Pharmaceuticals Inc

Sponsor: NOVEN PHARMS INC. Form: SYSTEM. Route: TRANSDERMAL

full page →fda approvals ↗
›Nov 29, 2024device 510k643d agoSurgical Instrument Service and Savings, Inc. — Medline ReNewal Reprocessed Abbott Inquiry Steerable Diagnostic Catheter (510k cleared)

Product code: NLH. Advisory committee: Cardiovascular. Type: Traditional

full page →fda device 510k ↗
›Nov 29, 2024device 510k643d agoMovano Inc. Dba Movano Health — Evie Med Ring (510k cleared)

Product code: DQA. Advisory committee: Cardiovascular. Type: Traditional

full page →fda device 510k ↗
›Nov 29, 2024device 510k643d agoRuthless, LLC Dba Ruthless Spine — Ruthless Spine RJB (510k cleared)

Product code: QWL. Advisory committee: Orthopedic. Type: Special

full page →fda device 510k ↗
›Nov 29, 2024device 510k643d agoMedical Electronic Systems , Ltd. — YO Home Sperm Test (510k cleared)

Product code: POV. Advisory committee: Hematology. Type: Traditional

full page →fda device 510k ↗

Week of Dec 2, 2024

11
›Dec 2, 2024approval640d agoTECVAYLI (TECLISTAMAB-CQYV) — FDA approvalteclistamab

Sponsor: JANSSEN BIOTECH. Form: INJECTABLE. Route: INJECTION

full page →teclistamab →fda approvals ↗
›Dec 2, 2024approval640d agoTALVEY (TALQUETAMAB-TGVS) — FDA approvaltalquetamab

Sponsor: JANSSEN BIOTECH. Form: INJECTABLE. Route: INJECTION

full page →talquetamab →fda approvals ↗
›Dec 2, 2024approval640d agoAXTLE (PEMETREXED DIPOTASSIUM) — FDA approvalAXTLE

Sponsor: AVYXA HOLDINGS. Form: POWDER. Route: INTRAVENOUS

full page →AXTLE →fda approvals ↗
›Dec 2, 2024device 510k640d agoFlight Medical Innovations , Ltd. — Ventoux VC2; Ventoux VC3 (510k cleared)

Product code: CBK. Advisory committee: Anesthesiology. Type: Traditional

full page →fda device 510k ↗
›Dec 2, 2024device 510k640d agoMicro Therapeutics, Inc. d/b/a ev3 Neurovascular — Riptide™ Aspiration Pump; Riptide™ Collection Canister with Intermediate Tubing (510k cleared)

Product code: JCX. Advisory committee: General, Plastic Surgery. Type: Special

full page →fda device 510k ↗
›Dec 2, 2024device 510k640d agoPhilips Medical Systems Nederland B.V. — Philips IntelliSite Pathology Solution (510k cleared)

Product code: PSY. Advisory committee: Pathology. Type: Traditional

full page →fda device 510k ↗
›Dec 2, 2024device 510k640d agoSynthon Hispania S.L. — GripMate (510k cleared)

Product code: KZH. Advisory committee: General Hospital. Type: Traditional

full page →fda device 510k ↗
›Dec 2, 2024device 510k640d agoApira Science, Inc. — GroWell BT Hair Growth System (GW10042) (510k cleared)

Product code: OAP. Advisory committee: Physical Medicine. Type: Traditional

full page →fda device 510k ↗
›Dec 2, 2024device 510k640d agoSTERIS Corporation — enspire 3000 Cleaning and Liquid Chemical Sterilant Processing System (510k cleared)STERIS plc

Product code: FEB. Advisory committee: Gastroenterology, Urology. Type: Special

full page →fda device 510k ↗
›Dec 2, 2024device 510k640d agoIntravu, Inc. — MIDASVu (510k cleared)

Product code: HRX. Advisory committee: Orthopedic. Type: Traditional

full page →fda device 510k ↗
›Dec 2, 2024device 510k640d agoVilex, LLC — Hintermann Series H2 Total Ankle System (510k cleared)

Product code: HSN. Advisory committee: Orthopedic. Type: Traditional

full page →fda device 510k ↗
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