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. 955 recalls have been distributed to District of Columbia in the last 12 months.
Showing 29421–29440 of 47,654 recalls
Recalled Item: Custom Tray Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cataract Kit - Dr. Slingsby Recalled by Windstone Medical Packaging, Inc....
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENT Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minor Operation Kit Recalled by Windstone Medical Packaging, Inc. Due to AMS...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cataract Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eye Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Buffered Sodium Citrate: (9NC) Blood Collection Tubes Recalled...
The Issue: BD is initiating this product correction of multiple lots of BD Vacutainer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ophthalmic Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...
The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lumigan (bimatoprost ophthalmic solution) 0.01% Recalled by Allergan Sales,...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluphenazine Decanoate Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Divalproex Sodium Delayed Release Tablets Recalled by Zydus Pharmaceuticals...
The Issue: Failed Dissolution Specifications; 9 month long term stability
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by Sun Pharmaceutical Industries,...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...
The Issue: Intuitive Surgical has become aware and further investigation has determined...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 10MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9.5MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 10.5MM Product Number:...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 5.5MM Product Number: Recalled...
The Issue: Potential for the cutting blade to detach from the device and/or the distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.