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. 2,459 recalls have been distributed to District of Columbia in the last 12 months.
Showing 24561–24580 of 27,451 recalls
Recalled Item: STAR Excimer Laser System Recalled by Abbott Medical Optics, Inc. Due to...
The Issue: This corrective action will address an identified failure of the lamp and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTAX Endoscopic Accessories. OF-B194. Made in Japan. PENTAX Upper/Lower...
The Issue: PENTAX Medical has become aware of a product issue associated with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR Excimer Laser System Recalled by Abbott Medical Optics, Inc. Due to...
The Issue: This corrective action will address an identified failure of the lamp and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences EMBOL-X Glide Protection System Recalled by Edwards...
The Issue: Edwards Lifesciences is recalling certain lots of EMBOL-X Glide Protection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBAS INTEGRA 800 Analyzer with software 9864.C2 Cobas. COBAS Part Recalled...
The Issue: Roche COBAS INTEGRA 800 system, Software Version 9864.C2 does not perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAR Excimer Laser System with Variable Spot Scanning Recalled by Abbott...
The Issue: This corrective action will address an identified failure of the lamp and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NX3 Try-In Gel. The product is used as a tooth shade resin material....
The Issue: Kerr Corporation is voluntarily recalling one lot of NX3 Try-In Gel, because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: pH 7.0 Buffer Solution Pint and Quart Bottles Recalled by Mesa Laboratories,...
The Issue: Mesa Laboratories, Inc. is recalling certain lots of pH 7.0 Buffer Solution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Recalled by CooperSurgical,...
The Issue: CooperSurgical is recalling two lots of 900-863 because the wrong package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Nex Healing Abutment Recalled by Southern Implants, Inc Due to Southern...
The Issue: Southern Implants is recalling the Tri-Nex healing abutment because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAQUET Getinge Group CARDIOHELP Base Unit .7999 .8012 Recalled by Maquet...
The Issue: It has come to the attention of MAQUET that in certain rare instances, the...
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 recalling the Access 2 Immunoassay System because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Artis zee / zeego Angiography System is designed as Recalled by Siemens...
The Issue: There is a potential issue on running Artis systems running software VC1x...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rotoprone therapy System is an advanced patient care system Recalled by...
The Issue: The lock pin can become stuck in the "in" position during the manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P21x/5-1 MHz transducer Recalled by SonoSite, Inc. Due to FUJIFILM SonoSite...
The Issue: FUJIFILM SonoSite Inc. remove P21x/5-1 Transducer because the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harvest Graft Delivery System Recalled by Harvest Technologies Corporation...
The Issue: Potential for leur connector to leak or have cracks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Names: Integra¿ Camino 110-4 Intracranial Pressure (ICP) Monitoring...
The Issue: Integra LifeSciences has identified through an internal evaluation that in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIFY¿ Dual Species Self-Contained Biological Indicator Recalled by Steris...
The Issue: STERIS has identified that the population of the G. stearothermophilus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ready to Use Thymo-Cide Recalled by Wexford Labs Inc Due to Expired active...
The Issue: Expired active ingredient was used in the manufacture of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.