Recall data checked 8 hours ago

Loading recalls…

Loading…

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.

Home All recalls Services For shops For families Your account About Privacy Terms CPSC FDA NHTSA

Home › All recalls › Prescription medicine

Prescription medicine recalls

Prescription drugs recalled for contamination, potency or labelling.

Search recalls by product, brand or category

Or try another category

Everything

Children

Sleep & nursery274 Car seats254 Formula & baby food230 Children's medicine176 Swings & bouncers125 Nursery furniture317 Toys & play852 Strollers & carriers156 Clothing & sleepwear626

Adults & seniors

Prescription medicine2,003 Over-the-counter & supplements378 Mobility & home health182

Food & drink

Family food1,236

Pets

Pet food & products15

Home & car

Cleaning & chemicals271 Appliances & tools1,380 Furniture & furnishings572 Cars & vehicles12,233 Everything else2,312

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

2,003 recalls · newest first

Food & drug recall · FDAJanuary 18, 2024Serious

SUN PHARMACEUTICAL INDUSTRIES INC — Cinacalcet Tablets 60mg, Rx Only, 30 Tablets per bottle

Prescription medicine · SUN PHARMACEUTICAL INDUSTRIES INC · 1,728 bottles affected

CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.

Food & drug recall · FDAJanuary 18, 2024Labelling issue

Dr. Reddy's Laboratories, Inc. — Glimepiride Tablets, USP 1mg, 500-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam-532 409 INDIA, NDC: 55111-320-05

Prescription medicine · Dr. Reddy's Laboratories, Inc. · 14,425 bottles affected

Misprint on tablet

Food & drug recall · FDAJanuary 18, 2024Serious

SUN PHARMACEUTICAL INDUSTRIES INC — Niacin Extended-Release Tablets, USP 1000mg, Rx Only, 90 Tablets per bottle

Prescription medicine · SUN PHARMACEUTICAL INDUSTRIES INC · 6552 bottles affected

CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.

Food & drug recall · FDAJanuary 18, 2024Labelling issue

Dr. Reddy's Laboratories, Inc. — Glimepiride Tablets, USP 1mg, 100-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam-532 409 INDIA, NDC: 55111-320-01

Prescription medicine · Dr. Reddy's Laboratories, Inc. · 59,336 bottles affected

Misprint on tablet

Food & drug recall · FDAJanuary 18, 2024Serious

SUN PHARMACEUTICAL INDUSTRIES INC — Febuxostat Tablets 80 mg, Rx Only, 30 Tablets per bottle

Prescription medicine · SUN PHARMACEUTICAL INDUSTRIES INC · 19,992 bottles affected

CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.

Food & drug recall · FDAJanuary 18, 2024Serious

SUN PHARMACEUTICAL INDUSTRIES INC — Niacin Extended-Release Tablets, USP 500mg, Rx Only, 90 Tablets per bottle

Prescription medicine · SUN PHARMACEUTICAL INDUSTRIES INC · 15,768 bottles affected

CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.

Food & drug recall · FDAJanuary 17, 2024Serious

Henry Schein Inc. and Glove Club HSI Gloves Inc. — Adrenalin (epinephrine) Injection 1mg/mL, 1mL single dose vial, Rx only, Packaged By: Henry Schein, Inc., 80 Summit View Lane, Bastian, VA 24314, Original NDC 42023-159-25 Repack NDC 0404-9

Prescription medicine · Henry Schein Inc. and Glove Club HSI… · 1,099 Single Dose Vials affected

Labeling: Incorrect or Missing Lot and/or Exp Date.

Food & drug recall · FDAJanuary 16, 2024Serious

Den-Mat Holdings, LLC — OralProCare medicated lip treatment, Net Wt 9.9 g (0.35 oz) tube, Ethyl alcohol 6.0% Antibacterial

Prescription medicine · Den-Mat Holdings, LLC · 344 tubes affected

CGMP Deviations: products may not conform to the labeled specifications.

Food & drug recall · FDAJanuary 16, 2024Serious

Den-Mat Holdings, LLC — Hydrogen Peroxide Oral Rinse, Significantly Reduces Bacteria, Fresh Mint Flavor, Alcohol Free, a)16 fl. oz. (473 mL) bottle, NDC 59883-202-16, UPC 3 59883 00009 7); b) 64 fl. oz. (1.89 L) bottle, NDC 59883-202-64; c)

Prescription medicine · Den-Mat Holdings, LLC · 10,103 units affected

CGMP Deviations: products may not conform to the labeled specifications.

Food & drug recall · FDAJanuary 16, 2024Serious

Ascend Laboratories, LLC — Fosfomycin Tromethamine Granules for Oral Solution, (equivalent to 3 grams of fosfomycin), single-dose sachet, Rx Only

Prescription medicine · Ascend Laboratories, LLC · 71,244 sachets affected

Failed Impurities/Degradation Specification: Out of specification for organic impurities

Food & drug recall · FDAJanuary 15, 2024Serious

Amneal Pharmaceuticals of New York, LLC — Phenoxybenzamine Hydrochloride Capsules, USP 10mg, 100-count bottle, Rx only

Prescription medicine · Amneal Pharmaceuticals of New York, LLC · 858 bottles affected

Failed Impurities/Degradation Specifications: Out of specification for unknown impurity.

Food & drug recall · FDAJanuary 12, 2024Serious

IntegraDose Compounding Services LLC — Vasopressin 2 Unit/2 mL in 0.9% Sodium Chloride, 2 mL per syringe, Rx Only, 719 Kasota Ave SE, Minneapolis, MN. NDC 71139-0190-1

Prescription medicine · IntegraDose Compounding Services LLC · 281 syringes affected

Subpotent Drug

Food & drug recall · FDAJanuary 12, 2024Highest risk

Neptune Resources, LLC — Neptune's Fix, Tianeptine Extra Strength Elixir, 0.338 fl oz (10 mL) bottle

Prescription medicine · Neptune Resources, LLC · 117,000 bottles affected

Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.

Food & drug recall · FDAJanuary 12, 2024Serious

Golden State Medical Supply Inc. — Budesonide Extended-Release Tablets, 9 mg, 30-count bottles, Rx only

Prescription medicine · Golden State Medical Supply Inc. · 108 bottles affected

Failed Dissolution Specifications

Food & drug recall · FDAJanuary 12, 2024Highest risk

Neptune Resources, LLC — Neptune's Fix, Tianeptine Tablets Extended Relief, Twenty Tablets per Box, Wide Awake, 3000 mg (150 mg Per Tablet)

Prescription medicine · Neptune Resources, LLC · 4,932 boxes affected

Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.

Food & drug recall · FDAJanuary 12, 2024Highest risk

Neptune Resources, LLC — Neptune's Fix, Tianeptine Elixir, Fast Acting, 0.338 fl oz (10 mL) bottle

Prescription medicine · Neptune Resources, LLC · 1,000,000 bottles affected

Marketed without an approved NDA/ANDA: Product contains tianeptine, a substance not FDA-approved for any medical use in the United States.

Food & drug recall · FDAJanuary 11, 2024Serious

Par Sterile Products LLC — Vasostrict (vasopressin in 5% Dextrose) Injection, 20 units per 100 mL (0.2 units per mL), 100 mL x 10 Single Dose Vials per carton, Ready to Use, For Intravenous Infusion, Rx Only

Prescription medicine · Par Sterile Products LLC · 1721 cartons affected

Superpotent Drug: Assay from the 3-month and 6-month stability intervals exceeded the upper specification limit.

Food & drug recall · FDAJanuary 11, 2024Serious

Amerisource Health Services LLC — Rifampin Capsules USP, 150 mg, 30 Capsules (3 x 10) unit doses per carton, Rx Only

Prescription medicine · Amerisource Health Services LLC · 1,568 cartons affected

Failed Impurities/Degradation Specification.

Food & drug recall · FDAJanuary 10, 2024Serious

MEDLINE INDUSTRIES, LP - Northfield — Medline Remedy Clinical TREAT Antifungal Cream, 2% Miconazole Nitrate, Paraben Free, 4 FL OZ (118 mL) tube

Prescription medicine · MEDLINE INDUSTRIES, LP - Northfield · 1,786 tubes affected

Labeling: Not Elsewhere Classified; Product labeling contains the claim of 'Paraben Free' while the product does in fact contain parabens as part of…

Food & drug recall · FDAJanuary 10, 2024Serious

BE PHARMACEUTICALS AG — Fosaprepitant for Injection 150 mg per vial, Sterile lyophilized powder for Intravenous use only after reconstitution and dilution, Single Dose Vial, Rx Only

Prescription medicine · BE PHARMACEUTICALS AG · 22,176 Vials affected

Lack of Sterility Assurance: Aseptic process simulation failure.

← NewerPage 80 of 101Older →