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. 2,727 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,727 in last 12 months

Showing 39814000 of 51,854 recalls

Medical DeviceNovember 4, 2024· Straight Smile, LLC

Recalled Item: BYTE Aligner System BYTE All-Day Aligner System BYTE Recalled by Straight...

The Issue: Virtual-only clinical workflow utilized for dental aligners and impression...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: SENSE Breast Coil 3.0T 7ch Recalled by Philips North America Llc Due to...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: dS Breast 16ch 1.5T Recalled by Philips North America Llc Due to Potential...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: Mammotrak Diagnostic Coil 1.5T Recalled by Philips North America Llc Due to...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: dS Breast 7ch 3.0T Recalled by Philips North America Llc Due to Potential...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: ST SENSE Breast Dx Coil Recalled by Philips North America Llc Due to...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: SENSE Breast Coil Recalled by Philips North America Llc Due to Potential...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: dS Breast 7ch 1.5T Recalled by Philips North America Llc Due to Potential...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: dS Breast 16ch 3.0T Recalled by Philips North America Llc Due to Potential...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: ST SENSE Breast Coil Recalled by Philips North America Llc Due to Potential...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: Mammotrak Interventional Coil 1.5T Recalled by Philips North America Llc Due...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: Mammotrak Diagnostic Coil 3.0T Recalled by Philips North America Llc Due to...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2024· Philips North America Llc

Recalled Item: Achieva TX Interventional Coil 3.0T Recalled by Philips North America Llc...

The Issue: Potential safety issue where a patient may be harmed while preparing for or...

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

Class II — Potential Health HazardOngoing
FoodNovember 1, 2024· The JM Smucker Company LLC

Recalled Item: Great Value Cinnamon Rolls 16.5oz Recalled by The JM Smucker Company LLC Due...

The Issue: Pieces of plastic in product

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 1, 2024· The JM Smucker Company LLC

Recalled Item: Great Value Cheese Danish 16.5 oz Recalled by The JM Smucker Company LLC Due...

The Issue: Pieces of plastic in product

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above...

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

Class II — Potential Health HazardOngoing
Refund