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 87218740 of 28,688 recalls

Medical DeviceDecember 13, 2021· Olympus Corporation of the Americas

Recalled Item: OER-Elite Endoscope Reprocessor-for use in cleaning and high-level...

The Issue: The detergent and alcohol tank tubing may have been incorrectly assembled in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2021· FEMSelect Ltd

Recalled Item: The EnPlace is a single use trans-vaginal pelvic floor repair Recalled by...

The Issue: Certain lots may not have been packaged wth the Channel Tube Limiter.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2021· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products VersaTips Recalled by Ortho-Clinical Diagnostics,...

The Issue: The lot has a shape deformity which may lead to a 16% reduction in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2021· Mallinckrodt Pharmaceuticals Ireland Ltd

Recalled Item: THERAKOS CELLEX Photopheresis Procedural Kit Recalled by Mallinckrodt...

The Issue: This recall was initiated to recover a Dunnage Case, which is a case of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2021· DIXI MEDICAL USA

Recalled Item: The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or...

The Issue: Potential deformation of the internal packaging (blister pack) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2021· DIXI MEDICAL USA

Recalled Item: The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or...

The Issue: Potential deformation of the internal packaging (blister pack) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2021· DIXI MEDICAL USA

Recalled Item: The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or...

The Issue: Potential deformation of the internal packaging (blister pack) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2021· DIXI MEDICAL USA

Recalled Item: The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or...

The Issue: Potential deformation of the internal packaging (blister pack) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2021· DIXI MEDICAL USA

Recalled Item: The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or...

The Issue: Potential deformation of the internal packaging (blister pack) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2021· DIXI MEDICAL USA

Recalled Item: The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or...

The Issue: Potential deformation of the internal packaging (blister pack) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2021· DIXI MEDICAL USA

Recalled Item: The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or...

The Issue: Potential deformation of the internal packaging (blister pack) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2021· DIXI MEDICAL USA

Recalled Item: The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or...

The Issue: Potential deformation of the internal packaging (blister pack) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2021· DIXI MEDICAL USA

Recalled Item: The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or...

The Issue: Potential deformation of the internal packaging (blister pack) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2021· Getinge Usa Sales Inc

Recalled Item: Vaporizer Sevoflurane Maquet Filling Recalled by Getinge Usa Sales Inc Due...

The Issue: A potential chemical degradation of Sevoflurane by Lewis acids (metal oxides...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 9, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: ARTISTE with syngo RT Therapist-linear accelerator systems to deliver X-Ray...

The Issue: Potential safety issue under specific preconditons that may result in a user...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2021· R82 A/S

Recalled Item: R82 by ETAC Push Brace for High-Low Recalled by R82 A/S Due to The chrome...

The Issue: The chrome surface of the push brace can crack during use, potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2021· Technomed Europe

Recalled Item: Disposable Subdermal Needle Electrode Recalled by Technomed Europe Due to...

The Issue: There is a high risk of the blue hub detaching from the corkscrew needle,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· Fresenius Medical Care Holdings, Inc.

Recalled Item: Novalung Sensor Box (F30000163) a component of Novalung Console (F30000162)-...

The Issue: Error messages 206 (yellow) and 208 (red) technical failure, flow...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE REV STEM SZ 10 Product Code: 110010600 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2021· DePuy Orthopaedics, Inc.

Recalled Item: GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100 Recalled by DePuy...

The Issue: Stems may have an undersized spigot bore diameter therefore separating the...

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

Class II — Potential Health HazardOngoing