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. 903 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
903 in last 12 months

Showing 49881–49900 of 51,854 recalls

DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Betamethasone Sodium Phosphate 6 mg/mL P Injection Recalled by New England...

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
DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Betamethasone Repository 6 mg/mL PF Injection and Betamethasone Repository 6...

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
DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Triamcinolone 10 mg/mL P Recalled by New England Compounding Center Due to...

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
DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Saline 10% and 3% Recalled by New England Compounding Center Due to Lack 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
DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Omnipaque 240mg/mL PF Recalled by New England Compounding Center Due to Lack...

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
DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Glycerin 100% PF Recalled by New England Compounding Center Due to Lack 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
DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Methylprednisolone Acetate 40 mg/mL Injection Recalled by New England...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Isovue 200 mg/mL PF and 300 mg/mL PF Recalled by New England Compounding...

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
DrugSeptember 26, 2012· New England Compounding Center

Recalled Item: Methylprednisolone Acetate (PF) 40 mg/ml Injection Recalled by New England...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 26, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Definium 5000 / 5220493 X-Ray System Recalled by GE...

The Issue: When quickly switching the protocols from AEC to Fixed under the same view,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Definium 5000/5220493-2 X-Ray System Recalled by GE...

The Issue: When quickly switching the protocols from AEC to Fixed under the same view,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2012· DeGotzen

Recalled Item: DeGotzen XRay unit XGenus Dental X-ray unit. Recalled by DeGotzen Due to It...

The Issue: It was discovered at the WEAC Labs method sample did not meet requirements...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2012· MOOG Medical Devices Group

Recalled Item: ***This recall is being conducted due to an incomplete recall Recalled by...

The Issue: This recall is the same issue for the FDA processed recall initiated by Moog...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Teleflex Medical

Recalled Item: Hem-o-lok Large Polymer Ligating Clips Recalled by Teleflex Medical Due to...

The Issue: Product is being recalled due to the possibility that the tray may contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Belmont Instrument Corporation

Recalled Item: Belmont Rapid Infuser Recalled by Belmont Instrument Corporation Due to Leak...

The Issue: Leak from a saline bag caused saline to drip along the back of the Rapid...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Battery Recalled by Terumo Cardiovascular Systems Corporation Due to Terumo...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Battery Recalled by Terumo Cardiovascular Systems Corporation Due to Terumo...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...

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

Class II — Potential Health HazardOngoing