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. 2,710 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,710 in last 12 months

Showing 65216540 of 51,854 recalls

FoodFebruary 27, 2024· THE COCA-COLA COMPANY

Recalled Item: Powerade Mountain Berry Blast - 20oz PET bottles 24 variety pack Recalled by...

The Issue: The potential presence of a foreign metal object in the product, i.e. a...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2024· THE COCA-COLA COMPANY

Recalled Item: Powerade Zero Fruit Punch - 20oz PET bottles 24 variety pack Recalled by THE...

The Issue: The potential presence of a foreign metal object in the product, i.e. a...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2024· THE COCA-COLA COMPANY

Recalled Item: Powerade Zero Mixed Berry - 20 oz PET bottles 24 variety pack Recalled by...

The Issue: The potential presence of a foreign metal object in the product, i.e. a...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2024· Roland Foods, LLC.

Recalled Item: Roland Tahini Recalled by Roland Foods, LLC. Due to Potential Salmonella...

The Issue: Product may be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 27, 2024· Howmedica Osteonics Corp.

Recalled Item: TRIDENTII PSL CLUSTER58F-Indicated for use in primary and revision patients...

The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2024· Howmedica Osteonics Corp.

Recalled Item: TRIDENTII PSL CLUSTER48D- Indicated for use in primary and revision Recalled...

The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2024· Howmedica Osteonics Corp.

Recalled Item: TRIDENTII HEMI CLUSTER66H- Indicated for use in primary and revision...

The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2024· Howmedica Osteonics Corp.

Recalled Item: TRIDENTII HEMI CLUSTER48D-indicated for use in primary and revision patients...

The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2024· Howmedica Osteonics Corp.

Recalled Item: TRIDENTII PSL CLUSTER52E- Indicated for use in primary and revision Recalled...

The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2024· Howmedica Osteonics Corp.

Recalled Item: TRIDENTII PSL CLUSTER64H- Indicated for use in primary and revision Recalled...

The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2024· Howmedica Osteonics Corp.

Recalled Item: TRIDENTII HEMI CLUSTER50D- Indicated for use in primary and revision...

The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2024· Howmedica Osteonics Corp.

Recalled Item: TRIDENTII HEMI CLUSTER52E-Indicated for use in primary and revision patients...

The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2024· Howmedica Osteonics Corp.

Recalled Item: TRIDENTII HEMI CLUSTER58F- Indicated for use in primary and revision...

The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2024· Howmedica Osteonics Corp.

Recalled Item: TRIDENTII HEMI CLUSTER44B- Indicated for use in primary and revision...

The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2024· Howmedica Osteonics Corp.

Recalled Item: TRIDENTII PSL CLUSTER50D- Indicated for use in primary and revision Recalled...

The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2024· Howmedica Osteonics Corp.

Recalled Item: TRIDENTII HEMI CLUSTER54E- Indicated for use in primary and revision...

The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz SE & CO. KG Recalled by Karl Storz Endoscopy Due to Inadequate...

The Issue: Inadequate reprocessing validation evidence

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2024· ConvaTec, Inc

Recalled Item: ConvaTec CarboFlex Recalled by ConvaTec, Inc Due to The product does not...

The Issue: The product does not meet sterility assurance level.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz SE & CO. KG Recalled by Karl Storz Endoscopy Due to Inadequate...

The Issue: Inadequate reprocessing validation evidence

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 27, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz SE & CO. KG Recalled by Karl Storz Endoscopy Due to Inadequate...

The Issue: Inadequate reprocessing validation evidence

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

Class II — Potential Health HazardOngoing