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. 1,024 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
1,024 in last 12 months

Showing 18381–18400 of 51,854 recalls

Medical DeviceSeptember 21, 2020· Smith & Nephew, Inc.

Recalled Item: 5.5MM Arthrogarde Hip Access Cannula Recalled by Smith & Nephew, Inc. Due to...

The Issue: The J Lock feature on the cannula body was manufactured incorrectly,...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2020· GE Healthcare, LLC

Recalled Item: Revolution Apex Recalled by GE Healthcare, LLC Due to There is a potential...

The Issue: There is a potential for a smudge artifact that could be suspect for...

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

Class II — Potential Health HazardOngoing
FoodSeptember 21, 2020· Wismettac Asian Foods, INC

Recalled Item: Shirakiku brand Black Fungus (Kikurage) Recalled by Wismettac Asian Foods,...

The Issue: California Department of Public Health sampled and tested Shirakiku brand...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 18, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS Icono Interventional Fluoroscopic X-Ray system - Product Usage:...

The Issue: There is a software problem which affects the DSA Roadmap application on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· GE Healthcare, LLC

Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...

The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· Getinge Group Logistics America, LLC

Recalled Item: Servo-i Ventilator Recalled by Getinge Group Logistics America, LLC Due to A...

The Issue: A potentially shorter than specified nebulizer connector may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· Quidel Corporation

Recalled Item: Sofia SARS Antigen FIA Package Insert The Sofia SARS Antigen Recalled by...

The Issue: Instructions for use in the package insert for SARS Antigen FIA test were...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· GE Healthcare, LLC

Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...

The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· GE Healthcare, LLC

Recalled Item: GE Datex-Ohmeda Avance CS2 Anesthesia System - Product Usage: intended...

The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· GE Healthcare, LLC

Recalled Item: 9100c NXT system - Product Usage: Device is licensed and Recalled by GE...

The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· GE Healthcare, LLC

Recalled Item: Aestiva/5 MRI Anesthesia System - Product Usage: The Aestiva/5 MRI Recalled...

The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· Genicon, Inc.

Recalled Item: A Li-Gator Single Use Laparoscopic Clip Applier Recalled by Genicon, Inc....

The Issue: Device malfunction causing the applier to jam, and clip loading failures.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· GE Healthcare, LLC

Recalled Item: GE Datex-Ohmeda Aisys CS2 Anesthesia System - Product Usage: is Recalled by...

The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· GE Healthcare, LLC

Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...

The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.

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

Class II — Potential Health HazardOngoing
DrugSeptember 17, 2020· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 120 Recalled by Acella Pharmaceuticals, LLC Due to Subpotent...

The Issue: Subpotent Drug: FDA analysis found these products to be less than the...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 17, 2020· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 15 Recalled by Acella Pharmaceuticals, LLC Due to Subpotent Drug:...

The Issue: Subpotent Drug: FDA analysis found these products to be less than the...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 16, 2020· Arbor Pharmaceuticals Inc.

Recalled Item: Nymalize (nimodipine) oral solution Recalled by Arbor Pharmaceuticals Inc....

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugSeptember 16, 2020· Perrigo Company PLC

Recalled Item: Albuterol Sulfate Inhalation Aerosol Recalled by Perrigo Company PLC Due to...

The Issue: Defective Delivery System: Sustained trend of failure to dispense complaints.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 16, 2020· Merit Medical Systems, Inc.

Recalled Item: MeritMedical Cultura Flex Swab Recalled by Merit Medical Systems, Inc. Due...

The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2020· Merit Medical Systems, Inc.

Recalled Item: Merit Medical Cultura Collection and Transport System Recalled by Merit...

The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...

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

Class II — Potential Health HazardOngoing