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. 2,360 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,360 in last 12 months

Showing 2568125700 of 27,558 recalls

Medical DeviceMarch 20, 2013· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: HORIBA ABX PENTRA 400 I.S.E. Module Recalled by Horiba Instruments, Inc dba...

The Issue: HORIBA Medical is informing all ABX PENTRA 400 Analyzer with I.S.E. Module...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2013· Hospira Inc.

Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to Some patients are...

The Issue: Some patients are obtaining access to the dosage reset codes required to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2013· Hospira Inc.

Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to Some patients are...

The Issue: Some patients are obtaining access to the dosage reset codes required to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2013· Accuray Incorporated

Recalled Item: Accuray CyberKnife System Medical Physicist Recalled by Accuray Incorporated...

The Issue: A defect on the master-side connector block of the pneumatic tool changer...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· LeMaitre Vascular, Inc.

Recalled Item: Glow 'N Tell 20 cm Tape: 1100-00 (100 strips) Recalled by LeMaitre Vascular,...

The Issue: Devices were not sealed correctly during the manufacturing process, and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Stent Guide: 1102-00 (100 strips) Recalled by LeMaitre Vascular,...

The Issue: Devices were not sealed correctly during the manufacturing process, and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Clorox Healthcare Holdings, LLC (dba HealthLink)

Recalled Item: HealthLink***BIOPSY PUNCHES*** Disposable manual instrument for skin biopsy....

The Issue: Due to lack of sterilization.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Clorox Healthcare Holdings, LLC (dba HealthLink)

Recalled Item: PSS Select medical products***Biopsy Punches*** Disposable manual instrument...

The Issue: Due to lack of sterilization.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Shimadzu Medical Systems

Recalled Item: Shimadzu Corporation - Mobile DaRt Evolution This device is a Recalled by...

The Issue: The recall was initiated because Shimadzu Corporation has identified a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Integra Burlington MA, Inc.

Recalled Item: Integra Ojemann Cortical Stimulator Recalled by Integra Burlington MA, Inc....

The Issue: If the headphone jack is in use during a surgical procedure with the OCS2...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Linvatec Corp. dba ConMed Linvatec

Recalled Item: HD Still Capture System ConMed Linvatec . Captures Recalled by Linvatec...

The Issue: The VP1600 HD Still Capture Image System is recalled due to an anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Hospira Inc.

Recalled Item: GemStar Pump - Battery Product Usage: The GemStar Pump is Recalled by...

The Issue: Battery level lower then 2.4 volts results in corrupt history log and loss...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 18, 2013· Hospira Inc.

Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...

The Issue: Pump shutting off during use without warning.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 18, 2013· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow-B Solution Recalled by NxStage Medical, Inc. Due to Mislabeling

The Issue: Product may be mislabeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Hospira Inc.

Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...

The Issue: Pump shutting off during use without warning.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 18, 2013· Hospira Inc.

Recalled Item: GemStar Pump - Battery Product Usage: The GemStar Pump is Recalled by...

The Issue: Battery level lower then 2.4 volts results in corrupt history log and loss...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 18, 2013· Clorox Healthcare Holdings, LLC (dba HealthLink)

Recalled Item: ARGENT SURGICAL SYSTEMS***BIOPSY Punches*** Disposable manual instrument for...

The Issue: Due to lack of sterilization.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2013· Acist Medical Systems

Recalled Item: ACIST Medical Systems Inc. The ACIST Angiographic Injection System is...

The Issue: ACIST Medical Systems is issuing a voluntary recall notice for three...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2013· Hospira Inc.

Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...

The Issue: The proximal and distal pressure sensor calibration can drift resulting in...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 15, 2013· Hospira Inc.

Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...

The Issue: The proximal and distal pressure sensor calibration can drift resulting in...

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

Class I — Serious Health HazardOngoing