Product Recalls in South Dakota

Product recalls affecting South Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to South Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,365 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,365 in last 12 months

Showing 2436124380 of 27,558 recalls

Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT PUNCH CEMENTED Size 4-7 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· Abbott Diabetes Care, Inc.

Recalled Item: FreeStyle Blood Glucose Test Strips Recalled by Abbott Diabetes Care, Inc....

The Issue: Certain lots of FreeStyle and FreeStyle Lite Blood Glucose Test Strips...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 18, 2013· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH CEMENTED Size 2-3 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 PUNCH NONCEMENTED 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 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 Strata II Shunt Assembly Kit Recalled by Medtronic Neurosurgery...

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· 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 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· 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· 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 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· 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· 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 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 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 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· 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