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. 1,004 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
1,004 in last 12 months

Showing 25061–25080 of 51,854 recalls

DrugOctober 17, 2018· Qualgen, LLC

Recalled Item: Estradiol 15mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 17, 2018· Qualgen, LLC

Recalled Item: Testosterone 25 mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 17, 2018· Qualgen, LLC

Recalled Item: Estradiol 10mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 17, 2018· Qualgen, LLC

Recalled Item: Estradiol 6 mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 17, 2018· Qualgen, LLC

Recalled Item: Testosterone 12.5mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 17, 2018· Qualgen, LLC

Recalled Item: Testosterone 87.5mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 17, 2018· Qualgen, LLC

Recalled Item: Estradiol 25mg pellet Recalled by Qualgen, LLC Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 16, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista 500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics has identified an issue with Dimension Vista...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Canon Medical System, USA, INC.

Recalled Item: Radrex-i X-Ray System (DRAD-3000E) TFP-4336W (Wireless FPD) Software...

The Issue: software malfunction; It was found when a user performs radiography using...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· ASO, LLC

Recalled Item: Family Wellness First Aid Sterile Gauze Pad 3 in x 3 in Recalled by ASO, LLC...

The Issue: Potential that gauze pads may not be fully sterilized

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista 1500 Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: Siemens Healthcare Diagnostics has identified an issue with Dimension Vista...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· MED-EL Elektromedizinische Gereate, Gmbh

Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...

The Issue: Devices were distributed despite the Helium-fine leak test results not being...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: (1) Argon Medical Devices Vascuclamp Recalled by Argon Medical Devices, Inc...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: (1) Argon Medical Devices Stopcocks Recalled by Argon Medical Devices, Inc...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· MED-EL Elektromedizinische Gereate, Gmbh

Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...

The Issue: Devices were distributed despite the Helium-fine leak test results not being...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· MED-EL Elektromedizinische Gereate, Gmbh

Recalled Item: MED EL Cochlear Implant System Recalled by MED-EL Elektromedizinische...

The Issue: Devices were distributed despite the Helium-fine leak test results not being...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices Plugs Recalled by Argon Medical Devices, Inc Due to...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices TRI-JECT Recalled by Argon Medical Devices, Inc Due to...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: (1) Argon Medical Devices Double Female LL Adapter Recalled by Argon Medical...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2018· Argon Medical Devices, Inc

Recalled Item: Argon Medical Devices Double Male LL Adapter Recalled by Argon Medical...

The Issue: The seal formed on the edge of the pouch may be incomplete, which could...

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

Class II — Potential Health HazardOngoing