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. 1,988 recalls have been distributed to District of Columbia in the last 12 months.
Showing 3781–3800 of 27,451 recalls
Recalled Item: Proclaim 7 Elite Implantable Pulse Generator Recalled by Abbott Medical Due...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim 5 Implantable Pulse Generator Recalled by Abbott Medical Due...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFIRE FILMARRAY Gastrointestinal (GI) Panel (30 test kit) Recalled by...
The Issue: Due to increase of false positive Vibrio/Vibrio Cholerae results when using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim Plus 5 Implantable Pulse Generator Recalled by Abbott...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim DRG Implantable Pulse Generator Recalled by Abbott Medical...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspire Model 3028 Recalled by Inspire Medical Systems Inc. Due to There is...
The Issue: There is a potential manufacturing defect which can lead to electrical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim Plus 5 Implantable Pulse Generator Recalled by Abbott...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim Plus 7 Implantable Pulse Generator Recalled by Abbott...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim 5 Elite Implantable Pulse Generator Recalled by Abbott Medical Due...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim XR 7 Implantable Pulse Generator Recalled by Abbott Medical...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim 7 Implantable Pulse Generator Recalled by Abbott Medical Due...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Proclaim 5 Implantable Pulse Generator Recalled by Abbott Medical Due...
The Issue: The duration between the implantable pulse generator reaching the elective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: US AquaA 900H-Typ USA-3 x 208v-Intended for the purification of Recalled by...
The Issue: Concentrate Flow was exceeding the maximum 19.9 bar set point. The standard...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KNEE ARTHROSCOPY PACK Catalog Number: MEKA12R Recalled by American Contract...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A610 Clinician Programmer (CP) Software Application (app) with the following...
The Issue: Patients implanted with a pocket adaptor (Model 64001 and/or 64002) are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventilator HAMILTON-C6 Recalled by Hamilton Medical AG Due to Ventilator may...
The Issue: Ventilator may enter sensor fail mode, ventilation may not re-initiate,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UPPER EXTREMITY PK Recalled by American Contract Systems Inc Due to Ethylene...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TOTAL KNEE - 302497- Procedure tray Catalog Number: ANTK12AF Recalled by...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAND PACK-Procedure Kit Catalog Number: WEHD16B Recalled by American...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTHROSCOPY WOLFSON PACK BHS Procedure tray Catalog Number: BPAR65A Recalled...
The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.