Product Recalls in South Carolina

Product recalls affecting South Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to South Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,671 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,671 in last 12 months

Showing 1350113520 of 28,688 recalls

Medical DeviceJuly 3, 2019· Valeritas, Incorporated

Recalled Item: DEMO No Needle Corrugated Carton 20 U/D Recalled by Valeritas, Incorporated...

The Issue: There is a potential for "No Needle Demo Units" to contain a needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Valeritas, Incorporated

Recalled Item: DEMO No Needle Corrugated Carton 30 U/D Recalled by Valeritas, Incorporated...

The Issue: There is a potential for "No Needle Demo Units" to contain a needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Valeritas, Incorporated

Recalled Item: DEMO No Needle Corrugated Carton 40 U/D Recalled by Valeritas, Incorporated...

The Issue: There is a potential for "No Needle Demo Units" to contain a needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Valeritas, Incorporated

Recalled Item: DEMO No Needle Corrugated Carton 20 U/D Recalled by Valeritas, Incorporated...

The Issue: There is a potential for "No Needle Demo Units" to contain a needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Valeritas, Incorporated

Recalled Item: DEMO No Needle Corrugated Carton 30 U/D Recalled by Valeritas, Incorporated...

The Issue: There is a potential for "No Needle Demo Units" to contain a needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Heidelberg Engineering GmbH

Recalled Item: SPECTRALIS with HEYEX2 image management system. a non-contact ophthalmic...

The Issue: Error in the default configuration which could lead to the incorrect display...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Siemens Medical Solutions USA, Inc

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

The Issue: Potential for four safety-related software issues impacting systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Drive Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for four safety-related software issues impacting systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for four safety-related software issues impacting systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Edge Plus Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for four safety-related software issues impacting systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Siemens Medical Solutions USA, Inc

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

The Issue: Potential for four safety-related software issues impacting systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Siemens Medical Solutions USA, Inc

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

The Issue: Potential for four safety-related software issues impacting systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Confidence Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Potential for four safety-related software issues impacting systems...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: CoolBlue Hyper-Hypothermia System- body hypothermia system Model: Innercool...

The Issue: Warnings statements have been added- exceeding 40 degree C for extended...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: Blanketrol III Hyper-Hypothermia System- body hypothermia system temperature...

The Issue: Warnings statements have been added- exceeding 40 degree C for extended...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Cincinnati Sub-Zero Products LLC, a Gentherm Company

Recalled Item: Blanketrol II Hyper-Hypothermia System Recalled by Cincinnati Sub-Zero...

The Issue: Warnings statements have been added- exceeding 40 degree C for extended...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: The Tina-Quant Myoglobin Gen. 2 Tests system is an immuno-turbidimetric...

The Issue: The firm conducted internal investigations that confirmed customer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Qiagen Sciences LLC

Recalled Item: QIAsymphony SP SOW 5.0.3 Recalled by Qiagen Sciences LLC Due to QIAsymphony...

The Issue: QIAsymphony software version 5.0.3 - Software issue incorreclty assigns the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151812 Recalled by...

The Issue: Cleaning processes potentially being ineffective

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2019· Zimmer Biomet, Inc.

Recalled Item: Orthopedic Salvage System (OSS) Hybrid Poly Tibia Item # 151811 Recalled by...

The Issue: Cleaning processes potentially being ineffective

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

Class II — Potential Health HazardOngoing