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calendar

29 catalysts · 12 device 510k · 10 recall · 7 approval

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  • device 510k12
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no tagged catalysts yet

Week of Feb 10, 2025

29
›Feb 12, 2025approval
565d ago
METHYLPREDNISOLONE ACETATE — FDA approvalMETHYLPREDNISOLONE ACETATE

Sponsor: SANDOZ. Form: INJECTABLE. Route: INJECTION

full page →METHYLPREDNISOLONE ACETATE →fda approvals ↗
›Feb 12, 2025approval565d agoMETHYLPREDNISOLONE ACETATE — FDA approvalMETHYLPREDNISOLONE ACETATE

Sponsor: SANDOZ. Form: INJECTABLE. Route: INJECTION

full page →METHYLPREDNISOLONE ACETATE →fda approvals ↗
›Feb 12, 2025approval565d agoIZERVAY (AVACINCAPTAD PEGOL SODIUM) — FDA approvalavacincaptad pegol sodium

Sponsor: ASTELLAS. Form: SOLUTION. Route: INTRAVITREAL

full page →avacincaptad pegol sodium →fda approvals ↗
›Feb 12, 2025approval565d agoPAXLOVID (COPACKAGED) (NIRMATRELVIR) — FDA approvalPAXLOVID (COPACKAGED)

Sponsor: PFIZER. Form: TABLET. Route: ORAL

full page →PAXLOVID (COPACKAGED) →fda approvals ↗
›Feb 12, 2025approval565d agoSELARSDI (USTEKINUMAB-AEKN) — FDA approvalAlvotech

Sponsor: ALVOTECH USA INC. Form: INJECTABLE. Route: INJECTION

full page →fda approvals ↗
›Feb 12, 2025approval565d agoVICTOZA (LIRAGLUTIDE) — FDA approvalSaxenda

Sponsor: NOVO NORDISK INC. Form: SOLUTION. Route: SUBCUTANEOUS

full page →Saxenda →fda approvals ↗
›Feb 12, 2025approval565d agoACETYLCYSTEINE — FDA approvalACETYLCYSTEINE

Sponsor: SOMERSET THERAPS LLC. Form: SOLUTION. Route: INHALATION, ORAL

full page →ACETYLCYSTEINE →fda approvals ↗
›Feb 12, 2025recall565d agoRemedyRepack Inc. recall (Cls II)RemedyRepack Inc

Carvedilol 25 mg Tablet, QTY: 30 Tablets per Blister Pack (3 x 10 blister cards), Rx Only, MFG by: Glenmark, Mahwah, NJ 07430, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC: 70518-3945-00. — Reason: CGMP deviations: presence of N-Nitroso Carvedilol Impurity-1 (NNC 1), above the FDA recommended acceptable intake limit. — Status: Terminated

full page →fda recalls ↗
›Feb 12, 2025recall565d agoPAI Holdings, LLC. dba Pharmaceutical Associates Inc recall (Cls III)Cosette Pharmaceuticals Inc

Guaifenesin and Codeine Phosphate Oral Solution USP, 100mg/10 mg per 5 mL, 16 fl oz (473 ml) bottles, PAI Pharmaceutical Associates, Inc., Greenville, SC 29605, NDC 0121-0775-16 — Reason: Superpotent; sodium benzoate preservative — Status: Completed

full page →fda recalls ↗
›Feb 12, 2025recall565d agoGlenmark Pharmaceuticals Inc., USA recall (Cls II)LB PHARMACEUTICALS INC

Carvedilol Tablets, USP, 12.5 mg, Rx only, a)500 Tablets, NDC 68462-164-05; b) 100 Tablets, NDC 68462-164-01, Manufactured for Glenmark Pharmaceuticals, NJ. — Reason: CGMP Deviations:N-Nitroso Carvedilol I impurity (NNCI-I) were found to be failing per current FDA recommended limit. — Status: Ongoing

full page →fda recalls ↗
›Feb 12, 2025recall565d agoGlenmark Pharmaceuticals Inc., USA recall (Cls II)LB PHARMACEUTICALS INC

Carvedilol Tablets, USP, 25 mg, Rx only, a)500 Tablets, NDC 68462-165-05; b) 100 Tablets, NDC 68462-165-01, Manufactured for Glenmark Pharmaceuticals, NJ. — Reason: CGMP Deviations:N-Nitroso Carvedilol I impurity (NNCI-I) were found to be failing per current FDA recommended limit. — Status: Ongoing

full page →fda recalls ↗
›Feb 12, 2025recall565d agoThe Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories recall (Cls II)Aurobindo Pharma USA Inc

Potassium Chloride Extended-Release Tablets, USP, 10 mEq (750 mg), 100 Tablets per carton (10 x 10 unit dose blisters), Rx Only, Distributed by: Aurobindo Pharma USA< INC., 279 Princeton-Hightstown Road, East Windsor, NJ 08520. Made in India. Distributed by: MAJOR PHARMACEUTICALS, Livonia, MI 48152. NDC: 0904-7216-61 — Reason: Failed Dissolution Specifications. — Status: Ongoing

full page →fda recalls ↗
›Feb 12, 2025recall565d agoTeva Pharmaceuticals USA, Inc recall (Cls II)Terns Pharmaceuticals, Inc.

Granix (tbo-filgrastim) Injection 300 mcg/0.5 mL, Single Dose prefilled syringe, packaged as a) 1 syringe in 1 CARTON, NDC 63459-910-11, Blister NDC 63459-910-12; (b)10 syringes in 1 CARTON, NDC 63459-910-15, Blister NDC 63459-910-12; (c) 1 syringe in 1 CARTON, NDC 63459-910-17 without safety guard and blister, Rx Only, Manufactured by: UAB Teva Baltics, Vilnius, Lithuania. Distributed by Teva Pharmaceuticals USA, Inc. North Wales PA 19454. Product of Israel. — Reason: Failed Stability Specifications - 12-month stability test result for one of the known peptides is below the specification limit — Status: Ongoing

full page →fda recalls ↗
›Feb 12, 2025recall565d agoENDO USA, Inc. recall (Cls I)Par Pharmaceutical Inc

Adrenalin Chloride Solution (Epinephrine Nasal Solution, USP), 30mg/30mL (1mg/mL), packaged in 30 mL vials, Distributed by: Par Pharmaceutical, Chestnut Ridge, NY 10977, NDC 42023-103-01 — Reason: Labeling: Not Elsewhere Classified: misleading label similar in appearance to the FDA-approved drug product Adrenalin¿ (epinephrine injection, USP) — Status: Ongoing

full page →fda recalls ↗
›Feb 12, 2025recall565d agoSKY PACKAGING recall (Cls II)Strides Pharma Science Ltd

HydrALAZINE Hydrochloride, 100 Tablets (10x10), USP, 50mg, Rx only, Manufactured by Strides Pharma Science Ltd, Bengaluru, India, Distributed by McKesson by: McKesson Corporation dba SKY Packaging, TN 38141. NDC 63739-328-10 — Reason: Failed Impurities/Degradation Specifications — Status: Ongoing

full page →fda recalls ↗
›Feb 12, 2025recall565d agoSKY PACKAGING recall (Cls II)Strides Pharma Science Ltd

HydrALAZINE Hydrochloride, 25 mg, 100 Unit Dose Tablets (10x10), USP, Rx only, Manufactured by Strides Pharma Science Ltd, Bengaluru, India, Distributed by McKesson by: McKesson Corporation dba SKY Packaging, TN 38141. NDC 63739-327-10 — Reason: Failed Impurities/Degradation Specifications — Status: Ongoing

full page →fda recalls ↗
›Feb 12, 2025recall565d agoFDC Limited recall (Cls II)FDC Ltd

Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, Maharashtra, India, Distributed by: Rising Pharmaceuticals Inc, New Jersey, NDC 64980-514-05. — Reason: Defective Container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle. — Status: Ongoing

full page →fda recalls ↗
›Feb 12, 2025device 510k565d agoKunshan Hi-Fortune Health Products Co., Ltd. — Electrically Powered Wheelchair (510k cleared)

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

full page →fda device 510k ↗
›Feb 12, 2025device 510k565d agoAspen Imaging Healthcare, Inc. — AspenView (510k cleared)

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

full page →fda device 510k ↗
›Feb 12, 2025device 510k565d agoKunshan Hi-Fortune Health Products Co., Ltd. — Electrically Powered Wheelchair (510k cleared)

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

full page →fda device 510k ↗
›Feb 12, 2025device 510k565d agoOpsens, Inc. — OptoMonitor 3 (510k cleared)

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

full page →fda device 510k ↗
›Feb 12, 2025device 510k565d agoSiemens Medical Solutions USA, Inc. — NAEOTOM Alpha.Peak/ NAEOTOM Alpha; NAEOTOM Alpha.Pro; NAEOTOM Alpha.Prime (510k cleared)

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

full page →fda device 510k ↗
›Feb 12, 2025device 510k565d agoSamsung Medison Co., Ltd. — V8 Diagnostic Ultrasound System; cV8 Diagnostic Ultrasound System; V7 Diagnostic Ultrasound System; cV7 Diagnostic Ultrasound System; V6 Diagnostic Ultrasound System; cV6 Diagnostic Ultrasound System (510k cleared)

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

full page →fda device 510k ↗
›Feb 12, 2025device 510k565d agoGi Bionics, LLC — Fecobionics Anorectal System (510k cleared)

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

full page →fda device 510k ↗
›Feb 12, 2025device 510k565d agoSubtle Medical, Inc. — SubtleHD (1.x) (510k cleared)

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

full page →fda device 510k ↗
›Feb 12, 2025device 510k565d agoQuality Electrodynamics, LLC — SureWave Elastography (Q7000225) (510k cleared)

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

full page →fda device 510k ↗
›Feb 12, 2025device 510k565d agoEtiometry, Inc. — Etiometry Platform (DAV 5.4 RAE 9.2) (510k cleared)

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

full page →fda device 510k ↗
›Feb 12, 2025device 510k565d agoBiokit, S.A. — ARCHITECT HSV-2 IgG, ARCHITECT HSV-2 IgG Calibrator, ARCHITECT HSV-2 IgG Controls (510k cleared)

Product code: MYF. Advisory committee: Microbiology. Type: Traditional

full page →fda device 510k ↗
›Feb 12, 2025device 510k565d agoZimmer, Inc. — Affixus Tibial Nailing System - 4mm screws (510k cleared)

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

full page →fda device 510k ↗
$TERN52.95-0.03%
$LBRX47.73-0.33%
$LBRX47.73-0.33%
$ALVO4.9500+1.43%
$NVO45.61-1.41%
$PFE27.96-0.21%