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. 1,044 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
1,044 in last 12 months

Showing 17701–17720 of 51,854 recalls

DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: ePHEDrine Sulfate 50 mg/10mL in 0.9% Sodium Chloride Injection Recalled by...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: Lidocaine HCl 2% 5 mL Recalled by SCA Pharmaceuticals Due to Lack of...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: Morphine Sulfate 30 mg/30 mL in 0.9% Sodium Chloride (1mg/ml) Recalled by...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: Ketamine 100 mg/10mL in 0.9% Sodium Chloride Injection (10 mg/mL) Recalled...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: fentaNYL 1500 mcg/30 mL (50 mcg/mL) Recalled by SCA Pharmaceuticals Due to...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: HYDROmorphone HCl 30 mg/30 mL in 0.9% Sodium Chloride Injection Recalled by...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: fentaNYL 100 mcg/50mL Bupivacaine HCl 0.125% in 0.9% Sodium Chloride 50 mL...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: Morphine Sulfate 3 mg/3 mL in 0.9% Sodium Chloride (1mg/mL) CII Recalled by...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class III — Low RiskOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: PHENYLephrine HCl 5000 mg/50 mL in Sodium Chloride 0.9% (100 mcg/mL) Rx Only...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: ePHEDrine Sulfate Recalled by SCA Pharmaceuticals Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2020· SCA Pharmaceuticals

Recalled Item: morphine sulfate 150 mg/30 mL in 0.9% Sodium Chloride Injection Recalled by...

The Issue: Lack of Assurance of Sterility; potential for a defective syringe cap,...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 16, 2020· US Compounding Inc

Recalled Item: Succinylcholine Chloride PF Inj. 200 mg/10 mL Recalled by US Compounding Inc...

The Issue: Labeling: Incorrect or Missing lot and/or expiration date: The lot number...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 16, 2020· Philips Ultrasound Inc

Recalled Item: Philips EPIQ Diagnostic Ultrasound System Recalled by Philips Ultrasound Inc...

The Issue: The manufacturer discovered an issue associated with the EPIQ Image Boost...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2020· Medtronic Neurosurgery

Recalled Item: X1 Recalled by Medtronic Neurosurgery Due to Neonatal Valves were...

The Issue: Neonatal Valves were manufactured with a ventricular catheter connection...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2020· Cook Medical Llc

Recalled Item: Disposable Humidification Flask Recalled by Cook Medical Llc Due to A small...

The Issue: A small percentage of the Disposable Humidification Flasks may have a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2020· Medtronic Neurosurgery

Recalled Item: X1 Recalled by Medtronic Neurosurgery Due to Neonatal Valves were...

The Issue: Neonatal Valves were manufactured with a ventricular catheter connection...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2020· Medtronic Neurosurgery

Recalled Item: X1 Recalled by Medtronic Neurosurgery Due to Neonatal Valves were...

The Issue: Neonatal Valves were manufactured with a ventricular catheter connection...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2020· Microbiologics Inc

Recalled Item: KWIK-STI(TM) Recalled by Microbiologics Inc Due to The expiration date on...

The Issue: The expiration date on the label of one component (negative control 0243U)...

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

Class III — Low RiskOngoing
Medical DeviceDecember 15, 2020· Boston Scientific Corporation

Recalled Item: ACUITY Universal Cutter Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific (BSC) is retrieving five Model 7060 ACUITY cutters...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2020· Penumbra Inc.

Recalled Item: Penumbra JET 7 KIT Reperfusion Catheter+Penumbra Hi-Flow Aspiration Tubing...

The Issue: The catheter may become susceptible to distal tip damage during use. Distal...

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

Class I — Serious Health HazardOngoing