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. 1,884 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
1,884 in last 12 months

Showing 2396123980 of 51,854 recalls

Medical DeviceMarch 29, 2019· GE Healthcare, LLC

Recalled Item: Precision 500D The Precision 500D R&F X-ray System is intended Recalled by...

The Issue: There has been a reported incident of a Distar CRT monitor that has fallen...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· Centurion Medical Products Corporation

Recalled Item: Sterile Nail Clipper Concave Edge (67710) Recalled by Centurion Medical...

The Issue: Compromised seal on the sterile barrier pouch.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2019· Centurion Medical Products Corporation

Recalled Item: Sterile Nail Nipper Recalled by Centurion Medical Products Corporation Due...

The Issue: Compromised seal on the sterile barrier pouch.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Philips North America, LLC

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...

The Issue: The MX40 may experience increased power consumption and may have a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Philips North America, LLC

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...

The Issue: The MX40 may experience increased power consumption and may have a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Philips North America, LLC

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...

The Issue: The MX40 may experience increased power consumption and may have a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Philips North America, LLC

Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America, LLC Due...

The Issue: The MX40 may experience increased power consumption and may have a lack of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Zimmer Biomet, Inc.

Recalled Item: T7 Driver Cannulated AO (Part Number 110018531) Product Usage: The Recalled...

The Issue: There is a potential of fracture, bending or shearing of the driver.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Zimmer Biomet, Inc.

Recalled Item: T7 Driver Solid AO (Part Number 110018541) Product Usage: The Recalled by...

The Issue: There is a potential of fracture, bending or shearing of the driver.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2019· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Recalled by Edwards Lifesciences, LLC Due to Difficulty...

The Issue: Difficulty with atrioseptostomy catheter balloon deflation after deployment,...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 28, 2019· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Recalled by Edwards Lifesciences, LLC Due to Difficulty...

The Issue: Difficulty with atrioseptostomy catheter balloon deflation after deployment,...

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

Class I — Serious Health HazardOngoing
FoodMarch 27, 2019· Theo Chocolate Inc

Recalled Item: Sea Salt 70% Dark Chocolate 3 oz. bars Recalled by Theo Chocolate Inc Due to...

The Issue: Theo Chocolate Sea Salt 70% Dark Chocolate Bar is recalled due to undeclared...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugMarch 26, 2019· Medi-Physics Inc. dba GE Healthcare

Recalled Item: Thallous Chloride TI 201 Injection Recalled by Medi-Physics Inc. dba GE...

The Issue: Chemical Contamination: Trace amounts of an impurity was detected in the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 26, 2019· Molnlycke Health Care, Inc

Recalled Item: EZ Derm Porcine Xenograft Recalled by Molnlycke Health Care, Inc Due to...

The Issue: Intermittent heat seal failures on the outer pouch of some EZ Derm products.

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

Class II — Potential Health HazardOngoing
DrugMarch 25, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Pravastatin Sodium Tablets USP Recalled by Glenmark Pharmaceuticals Inc.,...

The Issue: Presence Of Foreign Tablet: in a bottle of Pravastatin Sodium Tablets 20 mg.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 25, 2019· Hamilton Medical AG

Recalled Item: HAMILTON-G5 Recalled by Hamilton Medical AG Due to New software version for...

The Issue: New software version for affected ventilators reduces the probability of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 25, 2019· Change Healthcare Israel Ltd.

Recalled Item: McKesson Cardiology Hemo Recalled by Change Healthcare Israel Ltd. Due to...

The Issue: users are not notified of procedure medication discrepancies between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2019· Change Healthcare Israel Ltd.

Recalled Item: Horizon Cardiology Hemo Recalled by Change Healthcare Israel Ltd. Due to...

The Issue: users are not notified of procedure medication discrepancies between the...

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

Class II — Potential Health HazardOngoing
DrugMarch 22, 2019· InvaGen Pharmaceuticals, Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by InvaGen Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2019· InvaGen Pharmaceuticals, Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by InvaGen Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter.

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

Class II — Potential Health HazardOngoing
Refund