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. 981 recalls have been distributed to District of Columbia in the last 12 months.
Showing 21221–21240 of 47,654 recalls
Recalled Item: Go-EZ Screw 6.5x34 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire Single Trocar 2.5x170mm Recalled by BioPro, Inc. Due to Manufacturing...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go-EZ Screw 6.5x36 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go-EZ Screw 6.5x30 Recalled by BioPro, Inc. Due to Manufacturing flaw in the...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire HBS Sterile Lot Recalled by BioPro, Inc. Due to Manufacturing flaw in...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go-EZ Screw 6.5x100 Recalled by BioPro, Inc. Due to Manufacturing flaw in...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire Single Trocar 1.1x150mm Recalled by BioPro, Inc. Due to Manufacturing...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go-EZ Screw 6.5x105 Recalled by BioPro, Inc. Due to Manufacturing flaw in...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire Sterile Single Trochar Recalled by BioPro, Inc. Due to Manufacturing...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire Single Trocar 2.5x150mm Recalled by BioPro, Inc. Due to Manufacturing...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire HBS Sterile Recalled by BioPro, Inc. Due to Manufacturing flaw in the...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Go-EZ Screw 6.5x115 Recalled by BioPro, Inc. Due to Manufacturing flaw in...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-Wire Sterile Single Trochar .045 Recalled by BioPro, Inc. Due to...
The Issue: Manufacturing flaw in the sterile barrier system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iCT SP Model # 728311 Recalled by Philips Medical Systems (Cleveland) Inc...
The Issue: In certain instances when performing a cardiac step and shoot acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Model # 728321 Recalled by Philips Medical Systems...
The Issue: In certain instances when performing a cardiac step and shoot acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vereos PET/CT Model # 882446 Recalled by Philips Medical Systems (Cleveland)...
The Issue: In certain instances when performing a cardiac step and shoot acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IQon Spectral CT Model # 728332 Recalled by Philips Medical Systems...
The Issue: In certain instances when performing a cardiac step and shoot acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 Model # 728231 Recalled by Philips Medical Systems (Cleveland)...
The Issue: In certain instances when performing a cardiac step and shoot acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VOLUMAT MC AGILIA US Recalled by Fenwal Inc Due to The firm is correcting...
The Issue: The firm is correcting four software anomalies and KVO (keep vein open) end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vigilant Agilia Recalled by Fenwal Inc Due to The firm is correcting four...
The Issue: The firm is correcting four software anomalies and KVO (keep vein open) end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.