Product Recalls in Missouri

Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,918 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,918 in last 12 months

Showing 2258122600 of 29,298 recalls

Medical DeviceJuly 28, 2015· Beckman Coulter Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Leica Microsystems, Inc.

Recalled Item: The Leica ASP6025 Tissue Processor. Pathology and Hematology Departments....

The Issue: The ASP6025 Tissue Processor instrument is incorrectly getting into a state...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Siemens Healthcare Diagnostics, Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Trumpf Medical Systems, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Trumpf Medical Systems, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Cepheid

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.

Class III — Low RiskOngoing
Medical DeviceJuly 27, 2015· Cepheid

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.

Class III — Low RiskOngoing
Medical DeviceJuly 27, 2015· Trumpf Medical Systems, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Trumpf Medical Systems, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Trumpf Medical Systems, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

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.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2015· Transonic Systems Inc

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.

Class II — Potential Health HazardOngoing