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. 2,465 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,465 in last 12 months

Showing 2486124880 of 28,172 recalls

Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH CEMENTED Size 2-3 HP Recalled by...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH NONCEMENTED Size 2-3 Recalled...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH CEMENTED SIZE 1-1.5 Recalled by...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH NONCEMENTED Size 1-1.5 Recalled...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH NONCEMENTED Size 4-7 Recalled...

The Issue: DePuy Orthopaedics, Inc. is issuing a voluntary device correction of the HP...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· Medtronic Neurosurgery

Recalled Item: Medtronic Delta Shunt Assembly Kit with Bioglide Small Recalled by Medtronic...

The Issue: Medtronic Neurosurgery is recalling the CSF-Unitized Shunts, Delta Shunt...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2013· Medtronic Neurosurgery

Recalled Item: CSF-Unitized Shunt Recalled by Medtronic Neurosurgery Due to Medtronic...

The Issue: Medtronic Neurosurgery is recalling the CSF-Unitized Shunts, Delta Shunt...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2013· Intuitive Surgical, Inc.

Recalled Item: Mega Needle Driver Recalled by Intuitive Surgical, Inc. Due to Firm has...

The Issue: Firm has become aware of the potential for detachment of the jaw insert for...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2013· Instrumentation Laboratory Co.

Recalled Item: HemosIL Low Abnormal Control 2 UNASSAYED Part Number: 0020003220 Recalled by...

The Issue: HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2013· Intuitive Surgical, Inc.

Recalled Item: Large Needle Driver Recalled by Intuitive Surgical, Inc. Due to Firm has...

The Issue: Firm has become aware of the potential for detachment of the jaw insert for...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2013· Shimadzu Medical Systems

Recalled Item: Mobile X-ray System Recalled by Shimadzu Medical Systems Due to Shimadzu...

The Issue: Shimadzu Corporation is recalling the Shimadzu Mobile X-ray Sytems (MUX-100...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2013· Instrumentation Laboratory Co.

Recalled Item: HemosIL High Abnormal Control 3 UNASSAYED Part Number: 0020003320 Recalled...

The Issue: HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens SOMATOM Definition Recalled by Siemens Medical Solutions USA, Inc...

The Issue: During clinical operation, a malfunction may occur causing a system display...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2013· Instrumentation Laboratory Co.

Recalled Item: HemosIL Normal Control 1 UNASSAYED Part Number: 0020003120 Recalled by...

The Issue: HemosIL Low, Abnormal, Normal Controls UNASSAYED (no-value assigned) lacks...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Innova IGS 630. Biplane Cardiovascular and Interventional...

The Issue: GE Healthcare has recently become aware of a potential safety issue with...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2013· Smith & Nephew Inc.

Recalled Item: Renasys EZ Recalled by Smith & Nephew Inc. Due to Modification of the...

The Issue: Modification of the bacterial overflow guard (filter) and related changes to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2013· Accumetrics Inc

Recalled Item: VerifyNow IIb/IIIa Test Recalled by Accumetrics Inc Due to Accumetrics is...

The Issue: Accumetrics is recalling the VerifyNow IIb/IIIa 10-Test because it contains...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 14, 2013· Smith & Nephew Inc.

Recalled Item: Renasys EZ PLUS Recalled by Smith & Nephew Inc. Due to Modification of the...

The Issue: Modification of the bacterial overflow guard (filter) and related changes to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2013· Karl Storz Endoscopy America Inc

Recalled Item: Broncho Flexible Fiberscope Recalled by Karl Storz Endoscopy America Inc Due...

The Issue: KARL STORZ Endoscopy America, Inc. is recalling the Flexible Broncho...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2013· Instrumentation Industries Inc

Recalled Item: RTC 25-C Inline Aerosol Tee Adapter. Intended to be used Recalled by...

The Issue: Some packages of the RTC 25-C may have been shipped to customers with...

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

Class II — Potential Health HazardOngoing