foundmatterdb

Field reports on stuff that let you down

Medications

487 reports

Official feedMedications· FDA MedWatch safety alerts

Heart Pump Controller RecallThe maker or a government agency pulled this product. Check the model or lot number and stop using it until it's fixed or refunded.: Abiomed Removes Automated Impella Controllers Abiomed is removing Automated Impella Controllers due to purge cassette recognition failures that may lead to prolonged delayed in mechanical circulatory support.

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Official feedMedications· FDA MedWatch safety alerts

Convenience Kit Correction: Becton Dickinson Issues Correction for Kits and Procedure Trays Containing RecalledThe maker or a government agency pulled this product. Check the model or lot number and stop using it until it's fixed or refunded. Sodium Chloride Ampules BD is correcting convenience kits and procedural trays containing recalled Huons Co. sodium chloride ampules

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FDA recallMedicationsClass II· Safecor Health, LLC

Fluphenazine HCl Elixir, USP, 15 mg per 3 mL, Delivers: 10 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use Only, Rx Only, Pkg by: Safecor Health, Woburn, MA 01801. NDC: 00121-0653-04 Reason: Failed Stability Specifications Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · Nationwide in the USA.

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FDA recallMedicationsClass II· Safecor Health, LLC

Fluphenazine HCl Elixir, USP, 20 mg per 4 mL, Delivers: 10 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use Only, Rx Only, Pkg by: Safecor Health, Woburn, MA 01801. NDC: 00121-0653-04 Reason: Failed Stability Specifications Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · Nationwide in the USA.

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FDA recallMedicationsClass II· Safecor Health, LLC

Fluphenazine HCl Elixir, USP, 10 mg per 2 mL, Delivers: 10 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use Only, Rx Only, Pkg by: Safecor Health, Woburn, MA 01801. NDC: 00121-0653-04 Reason: Failed Stability Specifications Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · Nationwide in the USA.

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FDA recallMedicationsClass I· VITRUVIAS THERAPEUTICS INC

Thyroid Tablets, USP, 1/2 Grain (30 mg), Each tablet contains: levothyroxine (T4) 19 mcg, liothyronine (T3) 4.5 mcg, 100 Tablets, Rx only, Distributed by: Vitruvias Therapeutics, Auburn, AL 36830, Product of USA, NDC 69680-166-00. Reason: Superpotent Drug Class IThe FDA's most serious recall level: a reasonable chance the product could cause serious health problems or death. · Ongoing · US Nationwide.

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FDA recallMedicationsClass II· Safecor Health, LLC

Fluphenazine HCl Elixir, USP, 5 mg per 10 mL, Delivers: 10 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use Only, Rx Only, Pkg by: Safecor Health, Woburn, MA 01801. NDC: 00121-0654-16 Reason: Failed Stability Specifications Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · Nationwide in the USA.

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FDA recallMedicationsClass II· Safecor Health, LLC

Fluphenazine HCl Elixir, USP, 5 mg per 1 mL, Delivers: 10 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use Only, Rx Only, Pkg by: Safecor Health, Woburn, MA 01801. NDC: 00121-0653-04 Reason: Failed Stability Specifications Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · Nationwide in the USA.

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FDA recallMedicationsClass II· Safecor Health, LLC

Fluphenazine HCl Elixir, USP, 2.5 mg per 5 mL, Delivers: 5 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use Only, Rx Only, Pkg by: Safecor Health, Woburn, MA 01801. NDC: 00121-0654-16 Reason: Failed Stability Specifications Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · Nationwide in the USA.

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FDA recallMedicationsointmentAlternatives →Class II· SUN PHARMA /TARO

Lidocaine Ointment3 reports about ointment on this site. See them all → USP, 5%, Speermint Flavor, 50 g Jar, Rx only, Mfd. by: Taro Pharmaceuticals Inc., Brampton, Ontario, L6T1C, Canada, Dist By: Taro Pharmaceuticals U.S.A. Inc. Hawthorne NY 70532 NDC: 51672-3008-5 Reason: Failed Content Uniformity Specifications. Out of Specification for Assay during analysis at the 24- month long term stability station, at…

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FDA recallMedicationsClass II· Inventia Healthcare Limited

Chlorthalidone Tablets, USP, 25 mg, 100 Tablets per bottle, Rx only, Manufactured by: Inventia Healthcare Limited. NDC: 64980-599-01 Reason: Failed Dissolution Specifications Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · U.S. Nationwide

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FDA recallMedicationsClass II· Pfizer

Dopamine HCl Inj., USP, 200 mg/5 mL (40 mg/mL), 5 mL Single-dose, 25 vials per tray, Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA, Vial NDC 0409-5820-11, Carton NDC 0409-5820-01. Reason: Lack of Assurance of Sterility Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · US Nationwide.

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Official feedMedications· FDA MedWatch safety alerts

Early Alert: Heart Pump Controller Issue from Abiomed Abiomed is removing certain Impella Controllers with various hardware, firmware, and/or software updates based on a retrospective review of servicing records.

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FDA drug shortageMedications· Novo Nordisk, Inc.

Shortage: Liraglutide Injection — Liraglutide, Injection, 6 mg/1 mL (NDC 0480-3667-20) Status: Current Used for: Endocrinology/Metabolism

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FDA recallMedicationsClass II· OurPharma LLC

fentaNYL Citrate, 1,000 mcg/100 mL (10mcg/mL) Injection solution in 100 mL, 0.9% NaCl Bag, OurPharma LLC, 2512 S. City Lake, Fayetteville, AR, NDC 73013-1013-01. Reason: Labeling: Not Elsewhere Classified: Complaint received on 08/31/2026 regarding the discrepancy of the IV bag expiry (07/31/2026 and 11/30/2026) and the product expiry (12/09/2026). Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems.…

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FDA recallMedicationsClass III· ImprimisRx NJ LLC

Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution, 10 mL per dropper bottle, For Office Use Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-732-10 Reason: Subpotent Drug Class IIIThe lowest FDA recall level: unlikely to cause health problems, but it breaks the rules. · Ongoing · USA Nationwide

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FDA recallMedicationsClass I· American Regent, Inc.

Epinephrine Injection, USP, 30 mg/30 mL (1mg/mL), 30 mL-Multiple-Dose Vial, Rx Only, For Intravenous Infusion, intramuscular and Subcutaneous Use, AMERICAN REGENT INC., SHIRLEY, NY 11967. NDC 0517-3030-01 Reason: Presence of Particulate Matter and Lack of Assurance of Sterility. Particulate matter identified as nylon, cellulosic, acrylic, polyethylene and g…

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FDA recallMedicationsClass III· Ajanta Pharma USA Inc

Fluphenazine Hydrochloride Tablets, USP, 1mg, 100-count bottles, Rx Only, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807, Made in India, NDC 27241-255-01. Reason: Failed impurities/degradation specifications: (OOS) for Organic Impurities by HPLC (Impurity-A) during testing at the 18 months long term stability. Result: 1.1 percent. Spec: 1.0 per…

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FDA recallMedicationsClass I· Baxter Healthcare Corporation

Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL, 60016, Made in USA, NDC 00338-0719-06 Reason: Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution. Class IThe FDA's most serious recall level: a reasonable chance the product could cause serious health problems or death. · Ongoing · U.S. Nationwide.

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FDA recallMedicationsClass I· B BRAUN MEDICAL INC

0.9% Sodium Chloride Injection, USP, 100 mL Partial Fill in 150 mL PAB Container, Sterile, Rx only, B. Braun Medical Inc., Bethlehem, PA 18018 USA, NDC 0264-1800-32. Reason: Presence of Particulate Matter: particulate matter identified as iron oxide, inorganic material, cellulose cotton fiber or polystyrene Class IThe FDA's most serious recall level: a reasonable chance the product could cause serious health problems or death. · Ongoing · Nationwide within the United S…

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FDA drug shortageMedications· Novadoz Pharmaceuticals LLC

Shortage: Lisdexamfetamine Dimesylate Tablet, Chewable — Lisdexamfetamine Dimesylate, Tablet, Chewable, 30 mg (NDC 72205-134-91) Status: Current Used for: Psychiatry

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FDA drug shortageMedications· Novadoz Pharmaceuticals LLC

Shortage: Lisdexamfetamine Dimesylate Tablet, Chewable — Lisdexamfetamine Dimesylate, Tablet, Chewable, 20 mg (NDC 72205-133-91) Status: Current Used for: Psychiatry

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FDA drug shortageMedications· Accord Healthcare Inc.

Shortage: Dexmedetomidine Hydrochloride Injection — Dexmedetomidine Hydrochloride, Injection, 100 ug/1 mL (NDC 16729-239-93) Status: Current Reason: Discontinuation of the manufacture of the drug Used for: Anesthesia

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FDA drug shortageMedications· Chartwell Molecular Holdings LLC

Shortage: Flurazepam Hydrochloride Capsule — Flurazepam Hydrochloride, Capsule, 30 mg (NDC 62135-737-30) Status: Current Used for: Neurology, Other

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FDA drug shortageMedications· Chartwell Molecular Holdings LLC

Shortage: Flurazepam Hydrochloride Capsule — Flurazepam Hydrochloride, Capsule, 15 mg (NDC 62135-736-30) Status: Current Used for: Neurology, Other

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FDA drug shortageMedications· Chartwell Molecular Holdings LLC

Shortage: Flurazepam Hydrochloride Capsule — Flurazepam Hydrochloride, Capsule, 30 mg (NDC 62135-737-90) Status: Current Used for: Neurology, Other

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FDA drug shortageMedications· Medexus

Shortage: Triamcinolone Hexacetonide Injection — Hexatrione, Injection, 40 mg/2 mL (NDC 59137-570-01) Status: Current Used for: Rheumatology

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FDA drug shortageMedications· Somerset Therapeutics, LLC

Shortage: Bupivacaine Hydrochloride Injection — Bupivacaine Hydrochloride, Injection, 2.5 mg/1 mL (NDC 70069-752-01) Status: Current Used for: Anesthesia

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FDA drug shortageMedications· Somerset Therapeutics, LLC

Shortage: Atropine Sulfate Injection — Atropine Sulfate, Injection, 1 mg/1 mL (NDC 70069-641-25) Status: Current Used for: Anesthesia, Neurology, Pediatric

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FDA drug shortageMedications· Somerset Therapeutics, LLC

Shortage: Ropivacaine Hydrochloride Injection — Ropivacaine Hydrochloride, Injection, 5 mg/1 mL (NDC 70069-064-10) Status: Current Used for: Anesthesia

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