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. 2,612 recalls have been distributed to District of Columbia in the last 12 months.
Showing 9421–9440 of 27,451 recalls
Recalled Item: Atellica IM 1600 Analyzer- multi-component system for in vitro diagnostic...
The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer - multi-component system for in vitro Recalled by...
The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...
The Issue: Labeling does not include guidance for proper water-quality maintenance and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...
The Issue: Labeling does not include guidance for proper water-quality maintenance and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...
The Issue: Labeling does not include guidance for proper water-quality maintenance and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...
The Issue: Labeling does not include guidance for proper water-quality maintenance and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gore Propaten Vascular Graft configured for Pediatric Shunt Recalled by W L...
The Issue: Vascular Grafts containing an inner diameter of 6 mm may be incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gore Propaten Vascular Graft configured for Pediatric Shunt Recalled by W L...
The Issue: Vascular Grafts containing an inner diameter of 6 mm may be incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prime Fifth Wheel Stretcher-stretcher may be used for minor procedures...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proform- support surface is used to assist in the prevention Recalled by...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prime Big Wheel Stretcher-used as a short-term outpatient clinical...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S3 MedSurg Bed - intended to support and transport patients Recalled by...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Michael Graves with Stryker Highback Chair-intended for pediatric and adult...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InTouch 2131-intended to support a human patient in an acute care setting...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S3 MedSurg Bed - intended to support and transport patients Recalled by...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transport Stretcher 747 - a non-powered Recalled by Stryker Medical Division...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUB Pediatric Crib- intended to provide a pediatric patient support Recalled...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stretcher Chair-for use in all acute care hospitals and medical Recalled by...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ComfortGel - assists in the prevention and treatment of all Recalled by...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symmetry Plus Treatment Recliner - general hospital use as a Recalled by...
The Issue: Medical devices intended for use in a healthcare facility were distributed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.