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. 983 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
983 in last 12 months

Showing 35401–35420 of 51,854 recalls

FoodMay 2, 2016· CRF Frozen Foods, LLC

Recalled Item: Stew Vegetables Recalled by CRF Frozen Foods, LLC Due to Potential Listeria...

The Issue: Stew Vegetables are recalled because they have the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2016· CRF Frozen Foods, LLC

Recalled Item: Organic Multi-Colored Cauliflower Florets Recalled by CRF Frozen Foods, LLC...

The Issue: Organic Multi-Colored Cauliflower Florets are recalled because they have the...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2016· CRF Frozen Foods, LLC

Recalled Item: Organic Potato Medley Recalled by CRF Frozen Foods, LLC Due to Potential...

The Issue: Organic Potato Medley is recalled because it has the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2016· CRF Frozen Foods, LLC

Recalled Item: Organic Gardener's Blend Recalled by CRF Frozen Foods, LLC Due to Potential...

The Issue: Beans, Carrots, Corn, and Peas mixes are recalled because they have the...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2016· CRF Frozen Foods, LLC

Recalled Item: Supreme Fiesta Blend Recalled by CRF Frozen Foods, LLC Due to Potential...

The Issue: Supreme Fiesta Blend is recalled because it has the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2016· CRF Frozen Foods, LLC

Recalled Item: Harvest Vegetable Blend Recalled by CRF Frozen Foods, LLC Due to Potential...

The Issue: Harvest Vegetable Blend is recalled because it has the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2016· CRF Frozen Foods, LLC

Recalled Item: Supreme Stir-Fry Sensation Recalled by CRF Frozen Foods, LLC Due to...

The Issue: Supreme Stir-Fry Sensation is recalled because it has the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2016· CRF Frozen Foods, LLC

Recalled Item: Organic Steamers Roasted Red Potato & Vegetable Medley Recalled by CRF...

The Issue: Potoatoes, Beans, Peppers, and Mushrooms mixes are recalled because they...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2016· CRF Frozen Foods, LLC

Recalled Item: Organic Peas & Pearl Onions Recalled by CRF Frozen Foods, LLC Due to...

The Issue: Organic Peas & Pearl Onions are recalled because they have the potential to...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 2, 2016· Sandoz, Inc

Recalled Item: Dicloxacillin Sodium Capsules Recalled by Sandoz, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:Out of specification result for...

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

Class III — Low RiskOngoing
Refund
DrugMay 2, 2016· Sandoz, Inc

Recalled Item: Dicloxacillin Sodium Capsules USP Recalled by Sandoz, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:Out of specification result for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 2, 2016· Leica Biosystems Richmond Inc.

Recalled Item: CytoVision Image Analysis and Capture System Recalled by Leica Biosystems...

The Issue: Systems have an improperly activated Windows 7 OS, even though a valid...

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

Class III — Low RiskOngoing
Medical DeviceMay 2, 2016· Synthes (USA) Products LLC

Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 24 mm - Sterile...

The Issue: Labeling errors. The outer packge label expiration date may exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2016· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes 8.0 mm Flexible Shaft Reamer Recalled by Synthes (USA)...

The Issue: Devices did not pass the biological safety evaluation for cytotoxicity...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2016· AGFA Healthcare Corp.

Recalled Item: DX-D600 - DXD Imaging Package Recalled by AGFA Healthcare Corp. Due to One...

The Issue: One of the dent markers from the DX-D600 dropped down from the overhead rail.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2016· Synthes (USA) Products LLC

Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 30 mm - Sterile...

The Issue: Labeling errors. The outer packge label expiration date may exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2016· Synthes (USA) Products LLC

Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 35 mm - Sterile...

The Issue: Labeling errors. The outer packge label expiration date may exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare ADVIA Centaur Tnl-Ultra Assay . In-Vitro Diagnostic for...

The Issue: Exhibits a greater than 10% change in results in samples with biotin levels...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 CT Model 728231 Recalled by Philips Medical Systems...

The Issue: Software issues found in software versions v4.1.3/4.1.4/4.1.5 in the Philips...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT SP Model No. 728311 Recalled by Philips Medical Systems...

The Issue: Software issues found in v4.1 .3/4.1.5 in the Philips Brilliance iCT/ iCT SP...

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

Class II — Potential Health HazardOngoing