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 9601–9620 of 27,451 recalls
Recalled Item: T25 Cannulated Screwdrivers (CSD 025) packaged in Guide Wire Kits Recalled...
The Issue: Cannulated Screwdrivers may break at the driver tip along the shaft, near...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eyesuite 9.3.1 software Recalled by Haag-Streit USA Inc Due to Examination...
The Issue: Examination data and patient name may be mixed up when printing or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UpsylonTM Y Mesh Kit with Colpassist Vaginal Positioning Device - Recalled...
The Issue: Potential for pinholes (sterile barrier breach) on the edge of the pouch to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colpassist Vaginal Positioning Device - Product Usage: intended for use...
The Issue: Potential for pinholes (sterile barrier breach) on the edge of the pouch to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Illuminated Stepped Laser Probe Curved-for use in combination with 23G...
The Issue: Barcode label extended expiration date. Barcode located at the short side of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E3800 PC Units (spare parts) Recalled by Radiometer Medical ApS Due to Due...
The Issue: Due to an issue with the internal clock of the analyzers with an e3800 PC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiometer ABL90 FLEX Analyzer with E3800 PC units. The E3800 Recalled by...
The Issue: Due to an issue with the internal clock of the analyzers with an e3800 PC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiometer ABL90 FLEX PLUS Analyzer with E3800 PC units. The Recalled by...
The Issue: Due to an issue with the internal clock of the analyzers with an e3800 PC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access SARS-CoV-2 Antigen Recalled by Beckman Coulter Inc. Due to specimens...
The Issue: specimens collected in transport media may result is false negative results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRILLIANCE VOLUME system - A Computed Tomography X-Ray System intended...
The Issue: Cooling Unit (CLU) expelled out of a CT gantry of an iCT system may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VICI VENOUS STENT System Product Usage: is intended for the Recalled by...
The Issue: The firm has received reports of stent migration after implantation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VICI RDS VENOUS STENT System Product Usage: is indicated for Recalled by...
The Issue: The firm has received reports of stent migration after implantation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DONJOY ULTRASLING PRO ER/IR 30 Recalled by DJ Orthopedics de Mexico S.A. de...
The Issue: failed rivet at the chafe tab of arm sling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DONJOY ULTRASLING PRO AB Recalled by DJ Orthopedics de Mexico S.A. de C.V....
The Issue: failed rivet at the chafe tab of arm sling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DONJOY PRO Recalled by DJ Orthopedics de Mexico S.A. de C.V. Due to failed...
The Issue: failed rivet at the chafe tab of arm sling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DONJOY ULTRASLING PRO ER/IR 15 Recalled by DJ Orthopedics de Mexico S.A. de...
The Issue: failed rivet at the chafe tab of arm sling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERLA TL Lateral Connector Open - Product Usage: intended to Recalled by...
The Issue: Due to external labelling error/mix-up. Affected product external labels...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FISTULA ON-OFF KIT. Medical convenience kit Recalled by Avid Medical, Inc....
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIALYSIS ACCESS Medical convenience kit Recalled by Avid Medical, Inc. Due...
The Issue: Medical convenience kits are being recalled due to a potential breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COVID-19 Self-Test Kit *** INNOVA *** 3T Recalled by INNOVA MEDICAL GROUP,...
The Issue: Due to distributing test kits to customers who were not part of a clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.