Angiographic Catheter 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.: Boston Scientific Removes Imager II Angiographic Catheters Boston Scientific Imager II Angiographic Catheters removed due to a manufacturing issue leading to tip detachment; could result in procedural delays, embolism

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.

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

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.

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.

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.

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.

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.

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.

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.

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…

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

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.

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.

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

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.…

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

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…

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…

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.

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…

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

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

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

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

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

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

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

Clindamycin Injection USP in 5% Dextrose, 900 mg per 50 mL (12 mg/mL) in GALAXY 50 mL Single Dose Container, Rx only, Sterile Nonpyrogenic, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-3814-50. Reason: CGMP Deviations Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · US Nationwide; Puerto Rico; and Chile.

Vasopressin, in 0.9% Sodium Chloride Injection, 20 units per 100 mL (0.2 units/mL), 100mL Single-Dose Container, Rx only, Sterile, Baxter Healthcare Corporation, Deerfield, IL, 60012 USA, NDC 0338-9640-12. Reason: CGMP Deviations Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · US Nationwide; Puerto Rico; and Chile.