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. 1,026 recalls have been distributed to District of Columbia in the last 12 months.
Showing 14221–14240 of 47,654 recalls
Recalled Item: Chocolate & the Chip Gluten free original chocolate chip: Cookies: Recalled...
The Issue: Inspection by the California Department of Public Health found undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chocolate & the Chip The Big Cookie Cake Cookie cakes: Recalled by Chocolate...
The Issue: Inspection by the California Department of Public Health found undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chocolate & the Chip Lavender chocolate chip cookies: Cookies: 4 Recalled by...
The Issue: Inspection by the California Department of Public Health found undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chocolate & the Chip Brown Butter Rice Crispy Treat - Recalled by Chocolate...
The Issue: Inspection by the California Department of Public Health found undeclared...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled by Dr. Reddy's...
The Issue: Failed Excipient Specifications; product manufactured using an excipient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Omeprazole Delayed-Release Capsules Recalled by Dr. Reddy's Laboratories,...
The Issue: CGMP Deviations: Customer complaint for the presence of a staple co-mingled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled by Dr. Reddy's...
The Issue: Failed Excipient Specifications; product manufactured using an excipient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled by Dr. Reddy's...
The Issue: Failed Excipient Specifications and Presence of Foreign Tablets/Capsules;...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled by Dr. Reddy's...
The Issue: Failed Excipient Specifications; product manufactured using an excipient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled by Dr. Reddy's...
The Issue: Failed Excipient Specifications; product manufactured using an excipient...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Betaxolol Ophthalmic Solution Recalled by Akorn, Inc. Due to Microbial...
The Issue: Microbial Contamination of Sterile Products: Confirmed sterility failure...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SuperCore Biopsy Instrument: REF/Product Description: 701114090/SUPERCORE...
The Issue: Due to component (housing and plunger) detaching from the semi-automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cliquid MD version 3.4 software used in conjunction with Analyst Recalled by...
The Issue: The values of the Internal Standard (IS) concentrations are incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: .15.020 Recalled by Limacorporate S.p.A Due to There is a potential that the...
The Issue: There is a potential that the length of bone screws identified on labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: .15.010 Recalled by Limacorporate S.p.A Due to There is a potential that the...
The Issue: There is a potential that the length of bone screws identified on labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOTRIMIN AF (Miconazole nitrate 2%) Deodorant Powder Spray Recalled by Bayer...
The Issue: Chemical Contamination: presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray Recalled...
The Issue: cGMP Deviations: manufactured at the same facility where other lots were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lotrimin AF (Miconazole nitrate 2%) Liquid Spray NET WT 133g (4.6 oz) can...
The Issue: cGMP Deviations: manufactured at the same facility where other lots were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tinactin (Tolnaftate 1%) DEODORANT POWDER SPRAY NET WT 133g (4.6 OZ) can...
The Issue: Chemical Contamination: presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tinactin (Tolnaftate 1%) LIQUID SPRAY NET WT150g (5.3 OZ) can Recalled by...
The Issue: Chemical Contamination: presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.