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. 2,373 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,373 in last 12 months

Showing 2282122840 of 27,558 recalls

Medical DeviceOctober 7, 2014· Zimmer, Inc.

Recalled Item: The Persona Tibial Articular Surface Inserter is a sterilizable instrument...

The Issue: Affected product did not undergo heat treatment hardening step leading to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2014· Mako Surgical Corporation

Recalled Item: RESTORIS PST Acetabular Offset Shell Impactors An impactor is a Recalled by...

The Issue: MAKO has identified the potential that the shell impactors may be damaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2014· Mako Surgical Corporation

Recalled Item: RESTORIS PST Acetabular Straight Shell Impactors An impactor is a Recalled...

The Issue: MAKO has identified the potential that the shell impactors may be damaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2014· Mortara Instrument, Inc

Recalled Item: Mortara Surveyor S12 and Surveyor S19 Patient Monitors. Product Usage:...

The Issue: Martara Instrument, Inc. has recently became aware of a potential safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 7, 2014· Mako Surgical Corporation

Recalled Item: RESTORIS PST Straight Shell Inserter An impactor is a reusable Recalled by...

The Issue: MAKO has identified the potential that the shell impactors may be damaged...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· PEROUSE MEDICAL

Recalled Item: Synthes Inflation System (03.804.4135) Product Usage: Inflation system is...

The Issue: Additional instructions for use due to inability to raise the pressure above...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Elekta, Inc.

Recalled Item: Laksell Gamma Knife Perfexion Recalled by Elekta, Inc. Due to Elekta has...

The Issue: Elekta has become aware that the latches may be locked before they have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Baxter Healthcare Corp.

Recalled Item: HomeChoice Automated PD system and HomeChoice Pro Automated PD system...

The Issue: There are additional and updated warning and cautions that are not in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur BNP Assay for in vitro diagnostic use in Recalled by Siemens...

The Issue: Siemens Healthcare Diagnostics has confirmed that approximately 2000...

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

Class III — Low RiskOngoing
Medical DeviceOctober 6, 2014· Zimmer Surgical Inc

Recalled Item: UNIVERSAL Modular Electric/Battery Handpiece for surgery The electric...

The Issue: Non-injury complaints from Europe identified a malfunction that made it...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· PEROUSE MEDICAL

Recalled Item: Bard Caliber (CL3030) Inflation Device Product Usage: Inflation Device...

The Issue: Additional instructions for use due to inability to raise the pressure above...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Beckman Coulter Inc.

Recalled Item: Access 2 Immunoassay Systems Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is recalling the Small Form Factor Console PC (SFF PC)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Beckman Coulter Inc.

Recalled Item: UniCel DxC 600i SYNCHRON Access Clinical Analyzer Recalled by Beckman...

The Issue: Beckman Coulter is recalling the Small Form Factor Console PC (SFF PC)...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Microbiologics Inc

Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to This strain should be...

The Issue: This strain should be resistant to high levels of Gentamicin and be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Microbiologics Inc

Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to This strain should be...

The Issue: This strain should be resistant to high levels of Gentamicin and be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· Microbiologics Inc

Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to This strain should be...

The Issue: This strain should be resistant to high levels of Gentamicin and be...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· MWT Materials, Inc.

Recalled Item: Accusorb MRI MAC7007 Part Number: MRI-07 MRI-Breast Shield Product Usage:...

The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· MWT Materials, Inc.

Recalled Item: Accusorb MRI MAC7001 Part Number: MRI-01 MRI-Large Blanket Various Sizes...

The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· MWT Materials, Inc.

Recalled Item: Accusorb MRI MAC7002 Part Number: MRI-02 MRI-Arm Sleeve Various Sizes...

The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2014· MWT Materials, Inc.

Recalled Item: Accusorb MRI MAC7006 Part Number: MRI-06 MRI-Large Torso Wrap Product...

The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...

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

Class II — Potential Health HazardOngoing