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. 2,705 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,705 in last 12 months

Showing 88618880 of 51,854 recalls

DrugMay 25, 2023· Golden State Medical Supply Inc.

Recalled Item: Travoprost Ophthalmic Solution Recalled by Golden State Medical Supply Inc....

The Issue: Lack of Assurance of Sterility: Tamper Evidence Seal is missing on secondary...

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 25, 2023· ENTRINSIC HEALTH SOLUTION INC

Recalled Item: enterade Advanced Oncology Formula Recalled by ENTRINSIC HEALTH SOLUTION INC...

The Issue: Potential for the product to develop mold and spoil.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 25, 2023· Boston Scientific Corporation

Recalled Item: Flexiva Pulse 242 TracTip Single-Use Laser Fibers -intended to be Recalled...

The Issue: Manufactured with the incorrect component may result in lower power output...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2023· Boston Scientific Corporation

Recalled Item: Flexiva Pulse 242 TracTip Single-Use Laser Fibers - intended to Recalled by...

The Issue: Manufactured with the incorrect component may result in lower power output...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2023· Boston Scientific Corporation

Recalled Item: Flexiva Pulse ID-intended to be used as a device that Recalled by Boston...

The Issue: Manufactured with the incorrect component may result in lower power output...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2023· Boston Scientific Corporation

Recalled Item: Flexiva Pulse 242 Single-Use Laser Fibers-intended to be used as Recalled by...

The Issue: Manufactured with the incorrect component may result in lower power output...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2023· Boston Scientific Corporation

Recalled Item: Flexiva Pulse ID-intended to be used as a device that Recalled by Boston...

The Issue: Manufactured with the incorrect component may result in lower power output...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2023· Boston Scientific Corporation

Recalled Item: Flexiva Pulse 242 ID Trac Single Use Fiber-intended to be Recalled by Boston...

The Issue: Manufactured with the incorrect component may result in lower power output...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2023· Boston Scientific Corporation

Recalled Item: Flexiva Pulse ID 242 TracTip single Use Fiber-intended to be Recalled by...

The Issue: Manufactured with the incorrect component may result in lower power output...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Slick Set Uncuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy Recalled by...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal Murphy Eye Recalled by TELEFLEX LLC Due to...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Magill Recalled by TELEFLEX...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Pilling LOWSLEY PROSTATIC TRACTOR CVD Recalled by TELEFLEX LLC Due to There...

The Issue: There are incomplete pre-cleaning instructions within the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Pilling O'REILLY ESOPHAGEAL RETRACTOR Recalled by TELEFLEX LLC Due to There...

The Issue: There are incomplete pre-cleaning instructions within the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Pilling LOWSLEY PROSTATIC TRACTOR STR Recalled by TELEFLEX LLC Due to There...

The Issue: There are incomplete pre-cleaning instructions within the Instructions for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2023· QUIDEL CARDIOVASCULAR INC

Recalled Item: Quidel Triage Cardiac Panel: Recalled by QUIDEL CARDIOVASCULAR INC Due to...

The Issue: Raw material issue may cause cardiac panel products to have an average of...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by TELEFLEX LLC...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Murphy Recalled by TELEFLEX...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 25, 2023· TELEFLEX LLC

Recalled Item: Endotracheal Tube oral/nasal uncuffed/plain - Murphy Recalled by TELEFLEX...

The Issue: Reports of disconnection of the 15mm connector from the endotracheal tube...

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

Class I — Serious Health HazardOngoing