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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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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 · FDAJune 25, 2024Labelling issue

GLOBAL WIDGET LLC — Hemp Bombs CBD Pain Freeze (menthol 4%), 1000mg, 4 oz bottles

Prescription medicine · GLOBAL WIDGET LLC · 2082 bottles affected

Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.

Food & drug recall · FDAJune 24, 2024Labelling issue

Neilmed Pharmaceuticals Inc — SinuFrin Decongestant (oxymetazoline HCl) Nasal Solution Nasal Decongestant, Decongestant Relief for up to 12 Hours, 12 Hour Relief, 0.5 fl oz (15 ml) bottle

Prescription medicine · Neilmed Pharmaceuticals Inc · 20,370 bottles affected

Sub-potent Drug

Food & drug recall · FDAJune 24, 2024Serious

Amerisource Health Services LLC — buPROPion Hydrochloride Extended-release Tablets USP (XL) Once-Daily, 150 mg, 100 Tablets (10 x 10) per carton, Rx Only

Prescription medicine · Amerisource Health Services LLC · 2,484 cartons affected

Failed Dissolution Specifications; the product is dissolving faster than the specified limits.

Food & drug recall · FDAJune 21, 2024Serious

Zydus Pharmaceuticals (USA) Inc — Venlafaxine Hydrochloride Extended-Release Capsules, USP 37.5mg, packaged in a) 90-count bottles (NDC 68382-034-16) and b)1000-count bottles (NDC 68382-034-10), Rx only, Mfg. by: Zydus Lifesciences Ltd. Ahm

Prescription medicine · Zydus Pharmaceuticals (USA) Inc · a) 13,128 bottles; b) 252 bottles affected

Failed Dissolution Specifications: Out-of-specification results observed for dissolution testing at the 8-hour and 12-hour pull intervals.

Food & drug recall · FDAJune 20, 2024Serious

Little Moon Essentials LLC — Little Moon Essentials, Crampy Belly Rub (Camphor 1.1%), Packaged as a) 4 FL OZ (118ML) glass jar, UPC Code 6 73673 88260 2, NDC 70722-260-04; b) 2 FL OZ (59ML) glass jar, UPC Code 6 73673 88204 6, NDC 70722-260

Prescription medicine · Little Moon Essentials LLC · 788 glass jars affected

CGMP deviations

Food & drug recall · FDAJune 20, 2024Serious

Little Moon Essentials LLC — Little Moon Essentials, Aching Head Rub (Camphor 3.09%, Menthol 2.55%) , a) 0.5OZ (14G), metal tin, UPC Code 67367388226 8, NDC 70722-203-05; b)1OZ (28G) glass jar, UPC Code 6 73673 88203 9, NDC 70722-203-01; Li

Prescription medicine · Little Moon Essentials LLC · 6,312 tin and glass jars affected

CGMP deviations

Food & drug recall · FDAJune 20, 2024Serious

Little Moon Essentials LLC — Little Moon Essentials, Magical Muscle Oil, (Camphor 1.95%, Menthol 3.75%) packaged as: a) 2 FL OZ (59ML) glass jar, UPC Code 6 73673 88202 2, NDC 70722-246-02; b) 4 FL OZ (118ML) jar, UPC Code 6 73673 88233 6

Prescription medicine · Little Moon Essentials LLC · 1654 glass jars affected

CGMP deviations

Food & drug recall · FDAJune 20, 2024Serious

Little Moon Essentials LLC — Little Moon Essentials, Vital Vapor Balm, (Camphor 0.6%, Menthol 5.2%) Packaged as a) 0.5OZ (14G) metal tin, UPC Code 6 73673 88231 2, NDC 70722-229-05) b) 2OZ (57G) glass jar, UPC Code 6 73673 88220 6, NDC 7072

Prescription medicine · Little Moon Essentials LLC · 1041 affected

CGMP deviations

Food & drug recall · FDAJune 20, 2024Serious

Little Moon Essentials LLC — Little Moon Essentials, Ass Kisser, Packaged as a) 0.5 OZ (14G) metal tin, UPC Code 6 73673 88228 2, NDC 70722-208-05; b) 3 OZ (85.05G) metal tin, UPC Code 6 73673 88208 4, NDC 70722-208-03; Little Moon Essentia

Prescription medicine · Little Moon Essentials LLC · 165 metal tins affected

CGMP deviations

Food & drug recall · FDAJune 20, 2024Serious

Little Moon Essentials LLC — Little Moon Essentials, Asana Kisser, (Camphor 1.35%, Menthol 2.86%), Packaged as a) 0.5 OZ (14G) metal tin, UPC Code 6 73673 88227 5, NDC 70722-216-05; b) 3 OZ (85-05G) metal tin UPC Code 6 73673 88216 9, NDC 7

Prescription medicine · Little Moon Essentials LLC · 320 metal tins affected

CGMP deviations

Food & drug recall · FDAJune 20, 2024Serious

Little Moon Essentials LLC — Little Moon Essentials, Dream Cream (Camphor 0.45%, Menthol 5%), Packaged as a) 2OZ (57G) glass jar, UPC Code 6 73673 88214 5, NDC 70722-232-02; b) 4OZ (113G) glass jar, UPC Code 6 73673 88804 8, NDC 70722-232-0

Prescription medicine · Little Moon Essentials LLC · 1264 glass jars affected

CGMP deviations

Food & drug recall · FDAJune 18, 2024Serious

Fresenius Medical Care Holdings, Inc. — DELFLEX PERITONEAL DIALYSIS SOLUTION With LOW MAGNESIUM / LOW CALCIUM 4.25% DEXTROSE and attached stay "safe Exchange Set, 2500mL (Approx. 50 mL excess), Single Dose Container Sterile and Non-Pyrogeni

Prescription medicine · Fresenius Medical Care Holdings, Inc. · 183 cases affected

This product is being recalled due to the tube weld failure presents itself as a slow leak and can be difficult to detect.

Food & drug recall · FDAJune 18, 2024Labelling issue

Accord Healthcare, Inc. — Dodex Injectable (Cyanocobalamin Injection) USP, 1,000mcg/mL, 1mL multiple dose vial, Rx only

Prescription medicine · Accord Healthcare, Inc. · 52,998 affected

Subpotent drug: out of specification results

Food & drug recall · FDAJune 18, 2024Serious

The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories — Venlafaxine Hydrochloride, extended-release capsules, USP, 37.5mg, 10 x 10 blister card in one carton, Rx only, Mfg by: Cadila Healthcare Ltd., Ahmedabad, India

Prescription medicine · The Harvard Drug Group LLC dba Major… · 864 cartons affected

Failed dissolution specifications: out of specification result obtained during routine stability testing for high dissolution.

Food & drug recall · FDAJune 17, 2024Serious

Baxter Healthcare Corporation — Dianeal Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 2.5% Dextrose, For Intraperitoneal Administration Only, 6000 mL per bag, Rx Only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA. NDC

Prescription medicine · Baxter Healthcare Corporation · 6,874 bags affected

Lack of Assurance of Sterility: Potential presence of leaks originating from the Connector Assembly component.

Food & drug recall · FDAJune 17, 2024Serious

Trigen Laboratories — Methylphenidate Hydrochloride, Extended-release Tablets, USP, 36mg, 100-count Bottle, Rx Only

Prescription medicine · Trigen Laboratories · 10,448 100-count bottles affected

Failed dissolution specifications: this product is being recalled due to this batch not meeting dissolution specifications.

Food & drug recall · FDAJune 12, 2024Serious

PACIRA PHARMACEUTICALS INC — Zilretta (triamcinolone acetonide extended-release injectable suspension), 32 mg per vial, Rx only

Prescription medicine · PACIRA PHARMACEUTICALS INC · 40,517 kits affected

Failed Dissolution Specifications - did not meet the acceptance criteria for IVR Level 3 testing at 9 months 2-8¿C followed by 6 weeks at 25¿C

Food & drug recall · FDAJune 7, 2024Serious

Dr. Reddy's Laboratories, Inc. — Allopurinol Tablets, USP 300mg, 100 Tablets per bottle, Rx only

Prescription medicine · Dr. Reddy's Laboratories, Inc. · 20,520 units affected

Presence of foreign substance.

Food & drug recall · FDAJune 5, 2024Highest risk

Homeocare Laboratories, Inc. — STELLALIFE VEGA Oral Care, Spray, Unflavored, 1 fl oz (30 ml) bottles

Prescription medicine · Homeocare Laboratories, Inc. · 31,811 x 1 fl. oz. spray bottle affected

Microbial Contamination of Non-Sterile Products: multiple Bacillus species organisms

Food & drug recall · FDAJune 5, 2024Serious

Homeocare Laboratories, Inc. — STELLALIFE ADVANCED FORMULA Peppermint, VEGA Oral Care, Rinse, 16 fl oz (473 ml)

Prescription medicine · Homeocare Laboratories, Inc. · 31,110 x 16 fl. oz. bottle affected

Microbial Contamination of Non-Sterile Products: presence of Terribacillus species organism

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