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. 2,655 recalls have been distributed to District of Columbia in the last 12 months.
Showing 2741–2760 of 27,451 recalls
Recalled Item: MEDLINE convenience kits labeled as: 1) BURN Recalled by MEDLINE INDUSTRIES,...
The Issue: Medline is recalling medical convenience manufactured using certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE convenience kits labeled as: 1) LAKELAND SINGLE BASIN PACK-LF...
The Issue: Medline is recalling medical convenience manufactured using certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Imed Products Imed EVA BAG Recalled by The Metrix Company Due to A limited...
The Issue: A limited number of IV bags have been found to leak during filling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE convenience kits labeled as: PORT INSERTION PACK Recalled by MEDLINE...
The Issue: Medline is recalling medical convenience manufactured using certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SECURE 50 mL EMPTY EVA CONTAINER With 2 Ports Recalled by The Metrix Company...
The Issue: A limited number of IV bags have been found to leak during filling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE convenience kits labeled as: 1) GYN LAPAROSCOPY-LF Recalled by...
The Issue: Medline is recalling medical convenience manufactured using certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE convenience kits labeled as: 1) CIRCUMCISION PACK Recalled by...
The Issue: Medline is recalling medical convenience manufactured using certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORMIX 150 mL EMPTY EVA CONTAINER With 2 Ports Recalled by The Metrix...
The Issue: A limited number of IV bags have been found to leak during filling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE convenience kits labeled as: 1) TRACH TOTE Recalled by MEDLINE...
The Issue: Medline is recalling medical convenience manufactured using certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE convenience kits labeled as: 1) TOT/ GYN LITHOTOMY CDS Recalled by...
The Issue: Medline is recalling medical convenience manufactured using certain lots of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Imed Products Imed EVA BAG Recalled by The Metrix Company Due to A limited...
The Issue: A limited number of IV bags have been found to leak during filling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Approach Hydro ST Micro Wire Guide Recalled by Cook Incorporated Due to...
The Issue: Affected device lots have labels that state the incorrect expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Approach CTO Micro Wire Guide Recalled by Cook Incorporated Due to Affected...
The Issue: Affected device lots have labels that state the incorrect expiration dates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2. Model Numbers: FP2100X10 Recalled by Philips Respironics,...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo. Model Numbers: DS2110X11B Recalled by Philips Respironics, Inc....
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Zenition 70 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Potential for the Mains Control Unit board fuse may blow out during system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EV300. Model Numbers: DS2200X11B Recalled by Philips Respironics,...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Universal Ventilator. Model Number DS2000X11B. Intended for...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aeris EVO. Model Number: VT2110X24B. Intended for invasive and non-invasive...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Garbin Evo. Model Number: LD2110X23B. Intended for invasive and non-invasive...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.