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. 2,448 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,448 in last 12 months

Showing 2728127300 of 28,172 recalls

Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Interface module for CDl System 500 Product Usage: The Interface Recalled by...

The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Serial interface module RS-232 Product Usage: The System 1 provides Recalled...

The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· St. Jude Medical

Recalled Item: Eon - 3701 (Wall Charger) and 3711 (Portable Charger). Product Recalled by...

The Issue: St. Jude Medical has informed your doctor that a number of cases have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· St. Jude Medical

Recalled Item: Eon Mini - 3721 (Charger). Product Usage: Eon Mini system Recalled by St....

The Issue: St. Jude Medical has informed your doctor that a number of cases have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· St. Jude Medical

Recalled Item: Eon Mini - 3788 (IPG) Recalled by St. Jude Medical Due to As part of St....

The Issue: As part of St. Jude Medical's routine tracking and product monitoring, they...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2012· Aesculap Implant Systems LLC

Recalled Item: Aesculap S4 Element 4.5mm Polyaxial Screws (ST240T Recalled by Aesculap...

The Issue: There is a possibility that the screw channel that holds the rod in place...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 25, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Multi-Diluent 1 - Used for automated dilutions...

The Issue: Decrease in onboard dilution recovery when using Multi-Diluent 1 that has...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2012· Beckman Coulter Inc.

Recalled Item: Access Folate Calibrators Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is recalling the Access Folate Calibrators because it may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2012· DePuy Spine, Inc.

Recalled Item: DePuy Spine EXPEDIUM Offset Torque Wrench Product Code 2797-29-510 The...

The Issue: A component within the handle of the Expedium Offset Torque Wrench is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2012· Beckman Coulter Inc.

Recalled Item: Access Folate WHO Calibrators Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter is recalling the Access Folate Calibrators because it may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2012· Capintec Inc

Recalled Item: Capintec Captus 3000 Thyroid Uptake System Nuclear uptake probe intended...

The Issue: Customers who received a Capintec Captus 3000 Thyroid Uptake System with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2012· Cisco Systems Inc

Recalled Item: Cisco brand HealthPresence Recalled by Cisco Systems Inc Due to Software...

The Issue: Software anomaly may result in incorrect values and interpretations. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2012· Teleflex Medical

Recalled Item: TAUT Recalled by Teleflex Medical Due to Product is missing the label on the...

The Issue: Product is missing the label on the internal packaging.

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

Class III — Low RiskOngoing
Medical DeviceJuly 20, 2012· Galil Medical, Inc.

Recalled Item: Visual-ICE¿ Cryoablation System Recalled by Galil Medical, Inc. Due to Galil...

The Issue: Galil Medical is recalling a number of Visual Ice Cryoablation Systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 20, 2012· GE Healthcare, LLC

Recalled Item: CARESCAPE Monitor B850 Product Usage: The CARESCAPE TM Monitor B850 Recalled...

The Issue: GE Healthcare become aware of 4 potential issues associated with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 19, 2012· Abbott Point Of Care Inc.

Recalled Item: Cliniqa Liquid QCTM Cardiac Marker Control for i-STAT Level 1 Recalled by...

The Issue: Abbott Point of Care (APOC) has determined that for the Cliniqa Liquid QC...

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

Class III — Low RiskOngoing
Medical DeviceJuly 18, 2012· Siemens Medical Solutions USA, Inc

Recalled Item: syngo Imaging XS. Radiological image processing system. Recalled by Siemens...

The Issue: There is a potential malfunction when using syngo Imaging XS, version VA70A...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2012· Zimmer, Inc.

Recalled Item: Trabecular Metal Reverse Shoulder Liner 40mm Recalled by Zimmer, Inc. Due to...

The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2012· Zimmer, Inc.

Recalled Item: 00-4309-029-01 - Trabecular Metal Reverse Shoulder Liner 36 mm 65¿¿ Recalled...

The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2012· Zimmer, Inc.

Recalled Item: 00-4309-029-00- Trabecular Metal Reverse Shoulder Liner 36mm Recalled by...

The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...

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

Class II — Potential Health HazardOngoing