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. 2,496 recalls have been distributed to District of Columbia in the last 12 months.
Showing 18221–18240 of 27,451 recalls
Recalled Item: VITROS Chemistry Products UPRO Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: There is a potential for variable negatively and positively biased urine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/zeego Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens initiated a corrective action to address two possible, mutually...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIAMONDBACK 360 Peripheral 1.50 Classic Recalled by Cardiovascular Systems...
The Issue: CSI discovered that a 1.50mm Solid Crown OAD was labeled as a 1.50mm Crown OED.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Shaft L=120mm Recalled by Stanmore Implants Worldwide Ltd. Due to...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DF Coated Integral Shaft & Stem 15x30x38 Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Component Fixed Hinge Small Long Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medacta International SA Recalled by Medacta Usa Inc Due to Damaged...
The Issue: Damaged packaging, lack of sterility assurance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Integral Shaft & Stem 15x27 HA Coated Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Component Metal Cased Small Long Recalled by Stanmore Implants...
The Issue: The recalling firm has received 5 customer inquiries reporting that at least...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Electrophysiology Catheter Cables Catalog Number: CB3434CT...
The Issue: A breach in the sterile packaging may have occurred resulting in potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyberKnife Robotic Radiosurgery Systems Recalled by Accuray Incorporated Due...
The Issue: Accuray has become aware of a potential safety issue involving the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT Recalled by...
The Issue: A breach in the sterile packaging may have occurred resulting in potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System The product is used to manage Recalled by...
The Issue: Edits to Particle field definition parameters may not be saved when the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo One 5F Introducer Sheath 90 cm Product Code: HAL590 Recalled by BARD...
The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reunion TSA Peg Alignment Sound Catalog #5901-1038 The Peg Alignment...
The Issue: Reunion TSA Peg Alignment Sound broke during surgery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo One 5F Introducer Sheath 45 cm Product Code: HAL545 Recalled by BARD...
The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module Recalled by CareFusion 303, Inc. Due to During an...
The Issue: During an infusion, a false Air-in-Line (AIL) alarm would cause the infusion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halo One 5F Introducer Sheath 10 cm 5 pack Product Recalled by BARD...
The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K2M Special Connector Instruments (Special Connector Recalled by K2M, Inc...
The Issue: Instruments were developed without adequate consideration given to the need...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PreludeEASE Hydrophilic Sheath Introducer Dilator The Merit PreludeEASE...
The Issue: Recalling dilators included with the 6F PreludeEASE Hydrophilic Sheath...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.