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The Recall Registry is not a government service and does not issue recalls. We gather published recall notices from the U.S. Consumer Product Safety Commission, the U.S. Food and Drug Administration and the National Highway Traffic Safety Administration, and rewrite them in plain language. Always confirm the details with the issuing agency using the link on each recall page.

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Home › All recalls › Prescription medicine

Prescription medicine recalls

Prescription drugs recalled for contamination, potency or labelling.

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Highest riskSeriousWorth checkingLabelling issueTap any recall for the hazard and what to do

2,102 recalls · newest first

Food & drug recall · FDAMarch 19, 2026Serious

Teva Pharmaceuticals USA, Inc — Clonidine Transdermal System, USP, 0.2 mg/day, supplied in cartons of 4 Systems and 4 Adhesive Covers, Rx only

Prescription medicine · Teva Pharmaceuticals USA, Inc · 62,136 Cartons affected

CGMP Deviations: use of an unapproved raw material

Food & drug recall · FDAMarch 19, 2026Serious

Amneal Pharmaceuticals, LLC — traMADol Hydrochloride Tablets, USP, 50 mg, 500-count bottles, Rx only

Prescription medicine · Amneal Pharmaceuticals, LLC · 29,542 bottles affected

Failed Impurities/Degradation Specifications: N-nitroso-desmethyl-tramadol impurity (NDSRI) was found out of the specification at 24-month stability…

Food & drug recall · FDAMarch 18, 2026Highest risk

Amneal Pharmaceuticals, LLC — Magnesium Sulfate in Water for Injection, 4g/100 mL (40mg/mL) IV bag, further packaged in cartons of 12 x 100 mL IV bags, Rx only

Prescription medicine · Amneal Pharmaceuticals, LLC · 784 (12x100mL) cartons affected

Product mix up: a foil pouch labeled "Magnesium Sulfate in Water for Injection, 4 g/100 mL" actually contained an IV bag of Tranexamic Acid instead.

Food & drug recall · FDAMarch 18, 2026Labelling issue

Island Kinetics, Inc. d.b.a. CoValence Laboratories — Essential Calming Skin Gel, hydrocortisone 1%, 120mL/4oz net wt. (113g) per jar

Prescription medicine · Island Kinetics, Inc. d.b.a. CoValence… · 299 bottles affected

Subpotent Drug

Food & drug recall · FDAMarch 18, 2026Labelling issue

Island Kinetics, Inc. d.b.a. CoValence Laboratories — Remedy Gel, hydrocortisone 1%, 30 mL/ 1 fl oz per bottle

Prescription medicine · Island Kinetics, Inc. d.b.a. CoValence… · 1060 bottles affected

Subpotent Drug

Food & drug recall · FDAMarch 18, 2026Labelling issue

Island Kinetics, Inc. d.b.a. CoValence Laboratories — Skin Rehab, Calming Skin Gel, Hydrocortisone Balm, hydrocortisone 1%, .53oz net wt. (15.3g) per bottle

Prescription medicine · Island Kinetics, Inc. d.b.a. CoValence… · 2895 bottles affected

Subpotent Drug

Food & drug recall · FDAMarch 17, 2026Serious

Chiesi USA, Inc. — CUROSURF (poractant alfa), 240 mg, Intratracheal Suspension, 3L Single-dose-Vial, Rx only, Chiesi USA, Inc, Cary, NC 27518, NDC 10122-510-03.

Prescription medicine · Chiesi USA, Inc. · 7,235 vials affected

Lack of Assurance of Sterility

Food & drug recall · FDAMarch 17, 2026Serious

Teva Pharmaceuticals USA, Inc — Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 30 mg, Single-dose 8 mL vial in Kit, Rx only

Prescription medicine · Teva Pharmaceuticals USA, Inc · 21,930 Cartons affected

Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the…

Food & drug recall · FDAMarch 17, 2026Serious

Viatris, Inc. — Xanax XR, alprazolam, extended-release tablets, 3 mg, 60 Tablets bottles, Rx only

Prescription medicine · Viatris, Inc.

Failed Dissolution Specifications

Food & drug recall · FDAMarch 17, 2026Serious

Teva Pharmaceuticals USA, Inc — Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 20 mg, Single-dose 8 mL vial in Kit, Rx only

Prescription medicine · Teva Pharmaceuticals USA, Inc · 19,869 Cartons affected

Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the…

Food & drug recall · FDAMarch 17, 2026Serious

Teva Pharmaceuticals USA, Inc — Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 10 mg, Single-dose 8 mL vial in Kit, Rx only

Prescription medicine · Teva Pharmaceuticals USA, Inc · 1,897 Cartons affected

Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the…

Food & drug recall · FDAMarch 17, 2026Serious

Nephron SC, LLC — Albuterol Sulfate Inhalation Solution, 0.5%, 25 mg/5 mL (5 mg/mL*), 30x5 mL Sterile Unit-Dose Vials, Rx only, nephron 503B Outsourcing facility, 4600 12th Street Extension, West Columbia, SC 29172, NDC 69374-330-05.

Prescription medicine · Nephron SC, LLC · 146,280 vials affected

Labelling: Illegible label

Food & drug recall · FDAMarch 16, 2026Serious

Cipla USA, Inc. — Cinacalcet Hydrochloride Tablets, 90 mg, 30 Tablets per bottle, Rx Only

Prescription medicine · Cipla USA, Inc. · 63,192 bottles affected

CGMP Deviations; presence N-Nitroso Cinacalcet above the acceptable daily intake limit

Food & drug recall · FDAMarch 16, 2026Serious

Amerisource Health Services LLC — Meclizine Hydrochloride Tablets, USP 12.5 mg, (a) 50 Tablets [5 x 10] (NDC 60687-775-65) (b) 12.5 mg Individual Dose ( NDC 60687-775-11), Rx Only

Prescription medicine · Amerisource Health Services LLC · 697 cartons affected

Failed tablet specifications.

Food & drug recall · FDAMarch 16, 2026Serious

Cipla USA, Inc. — Cinacalcet Hydrochloride Tablets, 30 mg, 30 Tablets per bottle, Rx Only

Prescription medicine · Cipla USA, Inc. · 113,336 bottles affected

CGMP Deviations; presence N-Nitroso Cinacalcet above the acceptable daily intake limit

Food & drug recall · FDAMarch 16, 2026Serious

Cipla USA, Inc. — Cinacalcet Hydrochloride Tablets, 60 mg, 30 Tablets per bottle, Rx Only

Prescription medicine · Cipla USA, Inc. · 96,096 bottles affected

CGMP Deviations; presence N-Nitroso Cinacalcet above the acceptable daily intake limit

Food & drug recall · FDAMarch 13, 2026Serious

Cipla USA, Inc. — Lanreotide Injection, 120 mg/0.5 mL, Box contains 1 Pre-filled syringe, Single dose only, Rx Only

Prescription medicine · Cipla USA, Inc.

Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.

Food & drug recall · FDAMarch 13, 2026Serious

Cipla USA, Inc. — Lanreotide Injection, 120 mg*/0.5 mL, Box contains 1 Pre-filled syringe and 1 safety needle, Single dose only, Rx Only

Prescription medicine · Cipla USA, Inc. · 54,583 syringes affected

Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.

Food & drug recall · FDAMarch 13, 2026Serious

ENDO USA, Inc. — Buprenorphine Hydrochloride, Injection, 0.3mg/mL, 5x1 mL Single Dose Vials, Rx only

Prescription medicine · ENDO USA, Inc. · 34,293 vials affected

Crystallization; identified as Buprenorphine free base

Food & drug recall · FDAMarch 11, 2026Serious

Fresenius Kabi USA, LLC — 0.9% Sodium Chloride Injection, USP, 900 mg per 100 mL (9 mg per mL) 1,000 mL in a Single Dose freeflex bag, 1,000 mLx10, Fresenius Medical Care, Waltham, MA 02451

Prescription medicine · Fresenius Kabi USA, LLC

Lack of Assurance of Sterility

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