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. 2,438 recalls have been distributed to District of Columbia in the last 12 months.
Showing 35001–35020 of 47,654 recalls
Recalled Item: Kermit's Sweet & Tasty Key Lime Barbecue Sauce Recalled by Kermit, Inc. Due...
The Issue: Undeclared soy on product label
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kermit's Hot & Spicy Key Lime Barbecue Sauce Recalled by Kermit, Inc. Due to...
The Issue: Undeclared soy on product label
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kermit's Key Lime Cocktail Sauce Recalled by Kermit, Inc. Due to Undeclared Soy
The Issue: Undeclared soy on product label
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kermit's Key Lime Ginger Wasabi Marinade Recalled by Kermit, Inc. Due to...
The Issue: Undeclared soy and wheat on product label
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kermit's Chipotle Key Lime Barbecue Sauce Recalled by Kermit, Inc. Due to...
The Issue: Undeclared soy on product label
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kermit's Medium Mannered Key Lime Barbecue Sauce Recalled by Kermit, Inc....
The Issue: Undeclared soy on product label
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kermit's Key Lime Steak Sauce Recalled by Kermit, Inc. Due to Undeclared Soy
The Issue: Undeclared soy on product label
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medtronic Medical Device Identification Card for SureScan pacemaker...
The Issue: Some Medical Device Identification Cards provided to SureScan pacemaker...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 Computed Tomography X-ray systems. Intended to produce...
The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore (Oncology & Radiology) Computed Tomography X-ray...
The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Flex Computed Tomography X-ray systems. Intended to produce...
The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Computed Tomography X-ray systems. Intended to produce...
The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONSULT(TM) diagnostics hCG CONTROLS Kit Recalled by Biochemical Diagnostics...
The Issue: CONSULT diagnostics hCG Controls have discrepant storage temperatures listed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Computed Tomography X-ray systems. Intended to produce...
The Issue: The firm discovered Ring/Dot artifact due to X-ray measurement error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turon Shoulder Impaction Fixture The Turon and RSP Recalled by Encore...
The Issue: During the Turon assembly, the impaction forces caused the polymer, black...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORT-A-CATH Plastic Hub Needles Recalled by Smiths Medical ASD, Inc. Due to...
The Issue: The label on the lid stock of the individual needle packages for a portion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P/N: 9735023 Recalled by Medtronic Navigation, Inc. Due to Specific use...
The Issue: Specific use conditions can increase the possibility of a screwdriver tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P/N: 9734856 Recalled by Medtronic Navigation, Inc. Due to Specific use...
The Issue: Specific use conditions can increase the possibility of a screwdriver tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MILEX PESSARY KIT Recalled by CooperSurgical, Inc. Due to The products have...
The Issue: The products have been identified to have incorrect size prints on the MILEX...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reverse Shoulder Prosthesis Stem Impaction Fixture The Turon Recalled by...
The Issue: During the assembly, the impaction forces caused the polymer, black acetal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.