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. 2,485 recalls have been distributed to District of Columbia in the last 12 months.
Showing 21701–21720 of 47,654 recalls
Recalled Item: SIGNIA TRI-STAPLE 2.0 30MM MEDIUM/ THICK RELOAD Recalled by Covidien LLC Due...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EGIA 45 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EGIA 30 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNIA TRI-STAPLE 2.0 BLACK 60MM EXTRA THICK RELOA Recalled by Covidien LLC...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EGIA 60 CURVED TIP ART MED THICK SULU Recalled by Covidien LLC Due to The...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EGIA 60 ARTICULATING EXTRA THICK SULU Recalled by Covidien LLC Due to The...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNIA TRI-STAPLE 2.0 CURVED TIP 60MM MEDIUM/ THIC Recalled by Covidien LLC...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNIA TRI-STAPLE 2.0 BLACK 45MM EXTRA THICK RELOA Recalled by Covidien LLC...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EGIA 60 ARTICULATING MED THICK SULU Recalled by Covidien LLC Due to The...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EGIA45 CT AR MD THK REL Recalled by Covidien LLC Due to The device may be...
The Issue: The device may be missing one of two pin components that maintain alignment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Senographe Pristina - Product Usage: Senographe Pristina generates...
The Issue: Potential slippage of the biopsy positioner when the gantry is rotated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Pristina Serena - Product Usage: Pristina Serena is an Recalled by GE...
The Issue: Potential slippage of the biopsy positioner when the gantry is rotated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer 6.0 Is a device that displays medical Recalled...
The Issue: There is the possibility of viewing studies directly from the Enterprise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS Foundation Centricity PACS software product is intended for...
The Issue: There is the possibility of viewing studies directly from the Enterprise...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Immulox Recalled by APS BioGroup, Inc Due to The recall is being conducted...
The Issue: The recall is being conducted as a result of elevated APC levels. Through...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DPS Throat Spray Recalled by APS BioGroup, Inc Due to The recall is being...
The Issue: The recall is being conducted as a result of elevated APC levels. Through...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Viralox Recalled by APS BioGroup, Inc Due to The recall is being conducted...
The Issue: The recall is being conducted as a result of elevated APC levels. Through...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Immuno PRP Spray Recalled by APS BioGroup, Inc Due to The recall is being...
The Issue: The recall is being conducted as a result of elevated APC levels. Through...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 45cm Shaft PRODUCT CODE: NSLX145C...
The Issue: Observed reported incidence rate for harm associated with intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethicon ENSEAL X1 Curved Jaw Tissue Sealer 37cm Shaft PRODUCT CODE: NSLX137C...
The Issue: Observed reported incidence rate for harm associated with intraoperative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.