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. 2,386 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,386 in last 12 months

Showing 2238122400 of 27,558 recalls

Medical DeviceDecember 17, 2014· Stryker Craniomaxillofacial Division

Recalled Item: MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm Recalled by Stryker...

The Issue: Potential for implant damage, implant cracking off/breaking intra-operatively.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Stryker Craniomaxillofacial Division

Recalled Item: MEDPOR TITAN MAX Orbital Floor and Wall (OFW) MEDPOR-Titanium-Barrier (MTB)...

The Issue: Article #81036 (MEDPOR Titan Max OFW - MTB - Right) reportedly contained...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Aesculap, Inc.

Recalled Item: Miethke Shunt System accessories Product Usage: - The Miethke Shunt Recalled...

The Issue: Some Miethke Shunt System accessories may have an incorrect MR safety symbol...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Stryker Craniomaxillofacial Division

Recalled Item: MEDPOR BARRIER Sheets Orbital Floor Implant Product Usage: MEDPOR Implants...

The Issue: Potential for implant deformation, implant mechanical stability too low,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Stryker Craniomaxillofacial Division

Recalled Item: MEDPOR BARRIER Sheets Rectangle Product Usage: MEDPOR Implants in block...

The Issue: Potential for implant deformation, implant mechanical stability too low,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Zimmer Gmbh

Recalled Item: CoCr Femoral Head - indicated for hip arthroplasty for noncemented Recalled...

The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Zimmer Gmbh

Recalled Item: CoCr Femoral Head - A modular head component is used Recalled by Zimmer Gmbh...

The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Zimmer Gmbh

Recalled Item: Biolox Delta Femoral Head - The BIOLOX delta Ceramic Femoral Recalled by...

The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Zimmer Gmbh

Recalled Item: Metasul Femoral Head - indicated for total hip arthroplasty for Recalled by...

The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2014· Zimmer Gmbh

Recalled Item: Metasul Femoral Head - A modular head component is used Recalled by Zimmer...

The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2014· Leica Microsystems, Inc.

Recalled Item: Liquid Mouse Monoclonal Antibody CD15 used is laboratories to perform...

The Issue: The staining intensity decreases over the shelf life.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2014· Genetic Testing Institute,inc

Recalled Item: PF4 Concentrated Wash (10x) Recalled by Genetic Testing Institute,inc Due to...

The Issue: Some Lots of PF4 Concentrated Wash (10X) are a slightly more dilute...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2014· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Recalled by Beckman Coulter Inc. Due to N-Acetyl Cysteine...

The Issue: N-Acetyl Cysteine (NAC), when administered in therapeutic concentrations for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2014· Synthes, Inc.

Recalled Item: Malleable C- Retractor Recalled by Synthes, Inc. Due to Potential failure...

The Issue: Potential failure and/or corrosion of the internal spring of the retractor,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2014· Stryker Howmedica Osteonics Corp.

Recalled Item: Trident PSL HA Solid Back 50 mm Includes Dome Hole Recalled by Stryker...

The Issue: Five customer complaints were received for the same batch of Trident PSL...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2014· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Recalled by Beckman Coulter Inc. Due to N-Acetyl Cysteine...

The Issue: N-Acetyl Cysteine (NAC), when administered in therapeutic concentrations for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2014· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Recalled by Beckman Coulter Inc. Due to N-Acetyl Cysteine...

The Issue: N-Acetyl Cysteine (NAC), when administered in therapeutic concentrations for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2014· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Recalled by Beckman Coulter Inc. Due to N-Acetyl Cysteine...

The Issue: N-Acetyl Cysteine (NAC), when administered in therapeutic concentrations for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2014· NordicNeuroLab AS

Recalled Item: nordicTumorEx 1.0 nordicTumorEx is an image processing software package to...

The Issue: An error was discovered in the interpretation of certain DICOM header tags...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2014· Teleflex, Inc.

Recalled Item: R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal...

The Issue: Teleflex Medical has issued an advisory notification for the RUSCH Curved...

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

Class II — Potential Health HazardOngoing