Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,635 recalls have been distributed to District of Columbia in the last 12 months.
Showing 4501–4520 of 13,355 recalls
Recalled Item: Tropical Lip Moisturizer Recalled by Yusef Manufacturing Laboratories, LLC...
The Issue: Superpotent Drug: The beginning portion of the batch appears to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl
The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by The Harvard...
The Issue: CGMP Deviation: Potential presence of Nitrosodimethylamine (NDMA) Impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl
The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Koala Hand Sanitizer Recalled by Beaming White Llc Due to Undeclared Isopropyl
The Issue: Subpotent Drug: active ingredient ethanol tested below label claim and there...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clozapine Tablets USP tablet Recalled by Aurobindo Pharma USA Inc. Due to...
The Issue: Presence of foreign tablet: Consumer complaint of Clozapine Tablets 50mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irinotecan HCL Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...
The Issue: Defective Container: Customer complaints received of a crimp defect while...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irinotecan HCL Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...
The Issue: Defective Container: Customer complaints received of a crimp defect while...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nabumetone Tablets Recalled by American Health Packaging Due to Labeling Not...
The Issue: Labeling Not Elsewhere Classified: The statement Pharmacist: Dispense with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aripiprazole Tablets Recalled by Alembic Pharmaceuticals Limited Due to...
The Issue: Labeling: Label mix up: Bottles labeled as aripiprazole 2 mg, 30 count had...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Cream Recalled by Crown Laboratories Due to Subpotent Drug: Out of...
The Issue: Subpotent Drug: Out of specification for assay at the 9-month interval for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Cream Recalled by Crown Laboratories Due to Subpotent Drug: Out of...
The Issue: Subpotent Drug: Out of specification for assay at the 9-month interval for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prednisolone Sodium Phosphate Oral Solution Recalled by Akorn, Inc. Due to...
The Issue: Discoloration: Out of Specification (OOS) result for APHA Color Test.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Time-Cap Labs Recalled by Marksans Pharma Limited Due to CGMP Deviations:...
The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by AVKARE Inc. Due...
The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brimonidine Tartrate Opthalmic Solution 0.2% Recalled by SOMERSET...
The Issue: Failed Impurities/Degradation Specification: There is a slow leaching...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brimonidine Tartrate Opthalmic Solution 0.2% Recalled by SOMERSET...
The Issue: Failed Impurities/Degradation Specification: There is a slow leaching...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by AVKARE Inc. Due...
The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brimonidine Tartrate Opthalmic Solution 0.2% Recalled by SOMERSET...
The Issue: Failed Impurities/Degradation Specification: There is a slow leaching...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Soft Whisper by Powerstick Dandruff Shampoo (Pyrithione Zinc) Recalled by...
The Issue: cGMP Deviations: Soft Whisper Dandruff Shampoo was produced with water that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.