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 25721–25740 of 27,451 recalls
Recalled Item: VITEK 2 Compact computer system when equipped with the following Recalled by...
The Issue: There is a potential to link an isolate result to the wrong patient and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK 2 XL computer system when equipped with the following Recalled by...
The Issue: There is a potential to link an isolate result to the wrong patient and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK 2 60 computer system when equipped with the following Recalled by...
The Issue: There is a potential to link an isolate result to the wrong patient and then...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX Micros IM2 Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...
The Issue: Horiba Medical is recalling ABX Micros IM2 Data Management System because it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Molift Smart 150 Recalled by Moller Vital Due to The leg spreading mechanism...
The Issue: The leg spreading mechanism will fail to hoist and collapse if assemble...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Molift Smart 150 Recalled by Moller Vital Due to The leg spreading mechanism...
The Issue: The leg spreading mechanism will fail to hoist and collapse if assemble...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer C&S Transfer Straw Kit C&S Preservative Plus Urine Tube. 4.0...
The Issue: The BD Vacutainer Urinalysis Transfer Straw Kit #364991, Lot 1335484 has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Patient Helper Bed Frame Adapter Assembly The bed frame Recalled by...
The Issue: The bed frame adapter assemblies may have a weak weld where the patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxC 600i Synchron Access Clinical System Recalled by Beckman Coulter...
The Issue: Beckman Coulter is initiating a recall due to a defective newly released...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrapro Antipruritic Hydrogel Recalled by Oculus Innovative Sciences Inc Due...
The Issue: Out of specification result - stability test failure of free available...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Test Strips packaged in the OC-Light Manual iFOBT Kit Recalled by Polymedco,...
The Issue: The test strips in the affected product lots of the OC Light immunological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Test Strips packaged in the OC-Light Manual iFOBT Kit Recalled by Polymedco,...
The Issue: The test strips in the affected product lots of the OC Light immunological...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intellispace Portal (ISP) Philips Medical Systems (Cleveland) Recalled by...
The Issue: Philips was notified of a problem using the IntelliSpace Portal with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synchron LXi 725 Clinical System Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter is initiating a recall due to a defective newly released...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is initiating a recall due to a defective newly released...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access 2 Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is initiating a recall due to a defective newly released...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra(R) Jarit(R) Monopolar Cable (Catalogue No. 600-290). For use in...
The Issue: Addendum to the Instructions for Use. The addendum emphasizes the warnings...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO C and AMSCO 400 Steam Sterilizers designed for sterilization Recalled...
The Issue: The control boards alarm set points and temperature tolerances allowed for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System. Radiation treatment planning. Recalled by Elekta, Inc....
The Issue: The beam is displayed at the "gantry" angle, but the dose is calculated at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANTI-BORRELIA (LYME) MICROPLATE EIA Kit Recalled by Innominata Dba Genbio...
The Issue: Multiple incidents of low-reacting assay plates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.