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calendar

34 catalysts · 18 device 510k · 15 recall · 1 approval

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Week of Nov 25, 2024

34
›Nov 27, 2024approval
642d ago
WEGOVY (SEMAGLUTIDE) — FDA approvalNovo Nordisk AS

Sponsor: NOVO. Form: SOLUTION. Route: SUBCUTANEOUS

full page →fda approvals ↗
›Nov 27, 2024recall642d agoPadagis US LLC recall (Cls III)Padagis LLC

Triamcinolone Acetonide Cream USP, 0.025%, 1 LB (454 g) per jar, Rx Only, Manufactured By Padagis, Minneapolis, MN 55427. NDC: 45802-0063-05 — Reason: Subpotent and Superpotent Drug. Out of specification assay results recorded as part of Uniformity of Container test during long-term stability testing. — Status: Terminated

full page →fda recalls ↗
›Nov 27, 2024recall642d 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, 2024recall642d 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, 2024recall642d 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, 2024recall642d 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, 2024recall642d 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, 2024recall642d 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, 2024recall642d 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, 2024recall642d 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, 2024recall642d 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, 2024recall642d 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, 2024recall642d 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, 2024recall642d 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, 2024recall642d 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, 2024recall642d 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 510k642d 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 510k642d 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 510k642d 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 510k642d agoOntact Health Co., Ltd. — Sonix Health (510k cleared)

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

full page →fda device 510k ↗
›Nov 27, 2024device 510k642d 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 510k642d 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 510k642d 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 510k642d 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 510k642d 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 510k642d agoVilex, LLC — TACTIX Vector Syndesmosis System (510k cleared)

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

full page →fda device 510k ↗
›Nov 27, 2024device 510k642d 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 510k642d 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 510k642d 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 510k642d 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 510k642d 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 510k642d 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 510k642d 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 510k642d 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 ↗
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$ASBP
$LBRX47.73-0.33%
$LBRX47.73-0.33%
$RDY12.18+0.16%
$FRTRY
$ACBM
$LBRX47.73-0.33%
$NRXP
$CNMD32.58+1.46%