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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.
Showing 32201–32220 of 47,654 recalls
Recalled Item: OT1000 Series Orthopedic Surgical Tables Recalled by Steris Corporation Due...
The Issue: STERIS has identified that the pivot pin assembly located on the table top...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Proximal Foot/Left Recalled by Synthes (USA)...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Body with Left Foot/20mm Recalled by Synthes...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Body with Right Foot/20mm Recalled by Synthes...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Proximal Foot/Right Recalled by Synthes (USA)...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Body with Right Foot/30mm Recalled by Synthes...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Single Vector Distractor Body with Left Foot/30mm Recalled by Synthes...
The Issue: DePuy Synthes is voluntarily initiating a recall due to a possibility the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EV3 EverFiex" Self-expanding Peripheral Stent System Recalled by Ev3, Inc....
The Issue: Medtronic is issuing a medical device recall to return product potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMATE NUTRITION AMINO GOLD CAPSULES SUPER WHEY FORMULA Dietary Supplement...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ULTIMATE NUTRITION AMINO GOLD TABLETS SUPER WHEY FORMULA Dietary Supplement...
The Issue: Product contains undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Radiesse (+) Lidocaine Recalled by Merz North America, Inc. Due to...
The Issue: Complaints reported of Radiesse (+) unable to be expelled from the syringe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-wire Recalled by Integra LifeSciences Corp. Due to The affected K-wires do...
The Issue: The affected K-wires do not meet specification requirements. Specifically,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxycodone HCl Recalled by West-Ward Columbus Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specification; 9 month stability
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doxycycline Recalled by Galderma Laboratories, L.P. Due to Labeling:...
The Issue: Labeling: Incorrect Or Missing Lot and/or Exp Date: Some expiries and lot...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Toshiba Kalare DREX-KL80 X-ray generator Recalled by Toshiba American...
The Issue: It was discovered that the generator of the system could possibly terminate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Ultimax DREX-ULT80 X-ray generator Recalled by Toshiba American...
The Issue: It was discovered that the generator of the system could possibly terminate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conical portio adapter (acorn) small & large are used for Recalled by...
The Issue: The distal end of the Conical portio adapter (acorn) is composed of a small...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammotome Revolve Dual Vacuum Assist Biopsy System Model number: MST1009...
The Issue: A 10 Gauge needle, 9cm long was shipped in an 8 Gauge needle, 15 cm package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6534-08N InterActive¿ Implant Open-Tray Transfer Narrow Part Number:...
The Issue: The incorrect sized product, InterActive Implant Open-Tray Transfer Wide,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.