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 13301–13320 of 47,654 recalls
Recalled Item: Alinity s System software version2.8.0 Recalled by Abbott Laboratories, Inc...
The Issue: Software error associated with the immunoassay analyzer wash cycle which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: El Chavito¿ Saladitos Dried Salted Plums Recalled by El Chavito Due to...
The Issue: Potential to be contaminated with lead.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: El Chavito¿ Saladitos Enchilados Salted Plums with Chili Recalled by El...
The Issue: Potential to be contaminated with lead.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips StentBoost Live R2.0 application Recalled by Philips Healthcare Due...
The Issue: Due to an incorrect configuration setting in the EPX database of StentBoost...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura (Model Numbers 722010 Recalled by Philips North America Llc...
The Issue: Due to a software defect, the Philips StentBoost Live R2.0 might not process...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NuOss Collagen Block Size 8mm x 9mm x 9mm- used Recalled by Ace Surgical...
The Issue: NuOss Collagen (dental) was packaged with a Collatene Fibrillar Collagen(for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) JOBST Compri2 Recalled by BSN Medical Inc Due to Mislabeling
The Issue: The folding boxes within the shipping case are mislabeled. The shipping case...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mevion S250 and S250i Proton Therapy Systems hand pendant (P/N Recalled by...
The Issue: Malfunction of the hand pendant controlling movement of the therapy couch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC M/L Recalled by BioPro,...
The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MD Recalled by BioPro,...
The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium MPJ (Toe Implant)TOE JOINT TITANIUM NPC LG Recalled by BioPro, Inc....
The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MS Recalled by BioPro, Inc....
The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC SM Recalled by BioPro,...
The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC LG Recalled by BioPro, Inc....
The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium MPJ (Toe Implant)TOE JOINT TITANIUM PC SM Recalled by BioPro, Inc....
The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC ML Recalled by BioPro,...
The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MS Recalled by BioPro,...
The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MD Recalled by BioPro, Inc....
The Issue: There is an incorrect statement regarding MR Compatibility in the BioPro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFX-8000V. For radiographic and fluoroscopic studies and intervention....
The Issue: The fluoroscopic dose rate might exceed the conforming value during biplane...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ysiosystem with VC10 software version Recalled by Siemens Medical Solutions...
The Issue: Siemens Healthineers has identified a software error in previous software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.