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. 2,584 recalls have been distributed to District of Columbia in the last 12 months.
Showing 14001–14020 of 47,654 recalls
Recalled Item: Tastykake Creme Filled Krimpets 14.25oz (6-2ct) Recalled by Flowers Foods...
The Issue: The firm was notified by an ingredient supplier of the potential small metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tastykake Chocolate Creme Filled Cupcakes 14.25oz Recalled by Flowers Foods...
The Issue: The firm was notified by an ingredient supplier of the potential small metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tastykake Jelly Krimpets 12oz (6-2ct) Recalled by Flowers Foods (Corporate...
The Issue: The firm was notified by an ingredient supplier of the potential small metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tastykake Chocolate Cupcakes 12.75oz Recalled by Flowers Foods (Corporate...
The Issue: The firm was notified by an ingredient supplier of the potential small metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tastykake Buttercreme Iced Creme Filled Chocolate Cupcakes 14.25oz (6-2ct)...
The Issue: The firm was notified by an ingredient supplier of the potential small metal...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Diversatek Health Recalled by Diversatek Healthcare Due to M-Catch Retrieval...
The Issue: M-Catch Retrieval Nets, Part Number 1175-01 / Lot Number 001919, that were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wireless Footswtich used with the following Philips Allura Xper and Recalled...
The Issue: Wireless foot switch connection issues causing interruption of Fluoroscopy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System:...
The Issue: The Instructions for Use have been updated to include: (1) Clarification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clonidine Transdermal System Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MaryRuth's Organic Infants Liquid Probiotic Recalled by MARY RUTH ORGANICS...
The Issue: Internal testing found the presence of Pseudomonas aeruginosa in the product.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Orthopantomograph OP300 dental computed tomography x-ray system. The X-ray...
The Issue: It was noticed in production on 28.10.2021, that the final testing database...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsteoMed OsteoPower Power Console: -OsteoMed OsteoPower Power Console 2 by...
The Issue: Due to consoles not in compliance with the latest electrical safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cartia XT (Diltiazem Hydrochloride Extended-Release Capsules Recalled by...
The Issue: Labelling: Incorrect Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EVLP Convenience Pack/Kit Recalled by Medline Industries Inc Due to NaCl 250...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venous Access Pack-LF Convenience Kit Recalled by Medline Industries Inc Due...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Major Vascular CDS Convenience Kit Recalled by Medline Industries Inc Due to...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bedside PICC CDS Convenience Kit Recalled by Medline Industries Inc Due to...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuro Convenience Kit Recalled by Medline Industries Inc Due to NaCl 250 mL...
The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: artnaturals hand sanitizer Recalled by VIRGIN SCENT INC Due to CGMP...
The Issue: CGMP Deviations: Other lots recalled because they were manufactured using...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: artnaturals Hand Sanitizer Recalled by VIRGIN SCENT INC Due to CGMP...
The Issue: CGMP Deviations: Other lots recalled because they were manufactured using...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.