Product Recalls in Mississippi

Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,548 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,548 in last 12 months

Showing 1904119060 of 28,172 recalls

Medical DeviceSeptember 28, 2016· Baxter Healthcare Corp.

Recalled Item: V6 Rear Case Assembly Recalled by Baxter Healthcare Corp. Due to A...

The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Baxter Healthcare Corp.

Recalled Item: Baxter SIGMA Spectrum INFUSION PUMP with Master Drug Library Recalled by...

The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Zimmer Biomet, Inc.

Recalled Item: Zimmer¿ Gender Solutions" Patellofemoral Joint Prosthesis Milling Handpiece...

The Issue: Complaints have been reported that the handpiece is inoperable. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS 4F Stiffened Micro-Introducer Recalled by Angiodynamics, Inc....

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Baxter Healthcare Corp.

Recalled Item: sigma spectrum VOLUMETRIC INFUSION PUMP with Master Drug Library Recalled by...

The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: DOUBLE LINE KIT WITH 03ML FLUSH DEVICE FOR UNIVERSITY OF MICHIGAN HOSP....

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: TRIPLE PRESSURE KIT W/03ML FLUSH DEVICE FOR UNIV. OF IOWA Recalled by ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: Transpac¿ IV Monitoring Kit w/Arterial 84" Safeset" Reservoir Recalled by...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: CATH LAB KIT WITH 03ML FLUSH DEVICE FOR CARLE CLINIC Recalled by ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: TRANSPAC¿ IV BIFURCATED MONITORING KIT 72 INCH Recalled by ICU Medical, Inc....

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: TRANSPAC¿ IV MONITORING KIT WITH DISPOSABLE TRANSDUCER Recalled by ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· Advanced Sterilization Products

Recalled Item: EVOTECH Endoscope Cleaner and Reprocessor System 208V Recalled by Advanced...

The Issue: Advanced Sterilization Products (ASP) is recalling the EVOTECH Endoscope...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: Transpac¿ w/Safeset Reservoir Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: TRANSPAC¿ IV BIFURCATED KIT WITH SAFESET" RESERVOIR AND BLOOD SAMPLING PORTS...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing