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. 2,429 recalls have been distributed to District of Columbia in the last 12 months.
Showing 35601–35620 of 47,654 recalls
Recalled Item: CVS Pharmacy Recalled by Ohm Laboratories, Inc. Due to Superpotent Drug: Out...
The Issue: Superpotent Drug: Out Of Specification (OOS) result for Assay.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RAPIDPoint 500 Blood Gas Analyzer Recalled by Siemens Healthcare Diagnostics...
The Issue: When both ports (Serial and Ethernet) are configured to transmit data, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Thyroglobulin Assay Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter, Inc. is recalling Access Thyroglobulin reagent packs...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...
The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zippie IRIS Wheelchair. model EIZ5A in combination with option code Recalled...
The Issue: Quickie IRIS and Zippie IRIS tilt-in-space wheelchairs with MONO Backrest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...
The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xpert CT /NG Vaginal/Endocervical/ Specimen Collection Kit: Part number...
The Issue: Firm determined that some lots of CT/NG Swab 50 and CT/NG Urine collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...
The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ Folate Ascorbic Acid/Ascorbic Acid Diluent Recalled by...
The Issue: Low red blood cell control recoveries and low results for red blood cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xpert CT/NG Urine Specimen Collection Kit Part number GXCT/NGURINE-50...
The Issue: Firm determined that some lots of CT/NG Swab 50 and CT/NG Urine collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quickie IRIS Wheelchair. model EIZ4-2 in combination with option code...
The Issue: Quickie IRIS and Zippie IRIS tilt-in-space wheelchairs with MONO Backrest...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trumpf Ceiling Mounted Surgical Lighting Systems Recalled by Trumpf Medical...
The Issue: Complaints received of the front joint of the spring arm AC 2000 could break...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIDEX Activated Dialdehyde Solution Recalled by Advanced Sterilization...
The Issue: Advanced Sterilization Products (ASP) is recalling the CIDEX Activated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Flow Probe Recalled by Transonic Systems Inc Due to Software...
The Issue: Software defect; programming errors in the blood flow probes EPROM....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.