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 19021–19040 of 27,451 recalls
Recalled Item: CURVED-TIP STAPLER 30 Recalled by Intuitive Surgical, Inc. Due to Field...
The Issue: Field failures were reported related to the da Vinci Xi Surgical System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge RadSuite Recalled by Merge Healthcare, Inc. Due to It was reported by...
The Issue: It was reported by a customer that RadSuite images are not appearing as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...
The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Bone Level Implant Recalled by Straumann Manufacturing, Inc. Due...
The Issue: Misalignment with the Loxim transfer piece markings, the positioning of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS ZEE AND ZEEGO Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM Recalled by Siemens Medical Solutions...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIAISON Estradiol II Gen Recalled by Diasorin Inc. Due to DiaSorin is...
The Issue: DiaSorin is issuing an urgent medical device correction for the LIAISON¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Q AND Q.ZEN- MODULAR ANGIOGRAPHIC SYSTEM Recalled by Siemens Medical...
The Issue: The possibility exists for contaminants, in the form of biomass, to develop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quattro Air FFM MED AMER Recalled by Resmed Corporation Due to Masks in...
The Issue: Masks in this lot, labelled and sold as 62702 vented Quattro Air FFM size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Viva-ProE Systems Recalled by ELITech Group B.V. Due to Software...
The Issue: Software malfunction; The action being taken due to the device becoming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laseredge 1.1mm Arrow Knife Angled Recalled by Bausch & Lomb Inc Irb Due to...
The Issue: Possible dull knife edge
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laseredge Knife 1.5mm X 1.7mm TRAPEZOID ANGLED Recalled by Bausch & Lomb Inc...
The Issue: Possible dull knife edge
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trinity Biotech Captia Measles IgM Recalled by Clark Laboratories, Inc....
The Issue: The product lot failed to meet QC acceptance criteria during stability...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio2 PT/INR Professional Testing System Model Number: 0200431...
The Issue: Alere San Diego is initiating a voluntary recall for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio2 Replacement Monitor (Home) Model Number: 0200457 Product...
The Issue: Alere San Diego is initiating a voluntary recall for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio PT/INR System Professional Model Numbers: 0100004 Product...
The Issue: Alere San Diego is initiating a voluntary recall for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio Replacement Monitor Model Number: 0100137 Usage: The INRatio...
The Issue: Alere San Diego is initiating a voluntary recall for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio2 PT/INR Professional Monitoring System Model Number: 55128A...
The Issue: Alere San Diego is initiating a voluntary recall for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio2 PT/INR Home Monitoring System Model Number: 0200432 Recalled...
The Issue: Alere San Diego is initiating a voluntary recall for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio/ INRatio2 PT/INR Test Strips Model Number: 99007EU Recalled by...
The Issue: Alere San Diego is initiating a voluntary recall for the Alere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.