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. 2,652 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,652 in last 12 months

Showing 1480114820 of 28,688 recalls

Medical DeviceDecember 19, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity TF PET/CT (non-RoHS) Recalled by Philips Medical Systems...

The Issue: A software update is being issued to correct multiple issues identified in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Insulet Corporation

Recalled Item: Omnipod DASH Insulin Management System Recalled by Insulet Corporation Due...

The Issue: There is a potential for a communication interruption following a bolus...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: Aguja de Aspiracion con Profundidad Ajustable Tipo I 16ga x Recalled by...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: Aguja para Biopsia Tipo Medula Osea Ergonomica 11ga x 10cm Recalled by...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: J Type Bone Marrow Needle 13ga x 6cm - Product Recalled by Angiotech (Manan...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: Aguja de Aspiration con Profundidad Ajustable Tipo I 15ga x Recalled by...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: J Type Bone Marrow Needle 13ga x 10 cm- Product Recalled by Angiotech (Manan...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: "J" Type Bone Marrow Needle 11ga x 10 cm - Recalled by Angiotech (Manan...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2018· Angiotech (Manan Medical Products, Inc.)

Recalled Item: Double Diamond J Type Bone Marrow Needle & Marrow Extraction Recalled by...

The Issue: Argon Medical has identified an internal manufacturing issue on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Roche Diagnostics Corporation

Recalled Item: Lactate Gen.2 Recalled by Roche Diagnostics Corporation Due to New...

The Issue: New endogenous interference claims have been established for the following...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Roche Diagnostics Corporation

Recalled Item: Bilirubin Total Gen.3 Recalled by Roche Diagnostics Corporation Due to New...

The Issue: New endogenous interference claims have been established for the following...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Roche Diagnostics Corporation

Recalled Item: Tina-quant IgM Gen.2 Recalled by Roche Diagnostics Corporation Due to New...

The Issue: New endogenous interference claims have been established for the following...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus PCF-Q180AC Video Colonoscope - Product Usage: These endoscopes are...

The Issue: The adhesive used in the repair of the endoscope was incorrectly prepared....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus TJF-Q180V Duodenoscope - Product Usage: These endoscopes are...

The Issue: The adhesive used in the repair of the endoscope was incorrectly prepared....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus GIF-H180J Gastrointestinal Videoscope - Product Usage: These...

The Issue: The adhesive used in the repair of the endoscope was incorrectly prepared....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Olympus Corporation of the Americas

Recalled Item: Olympus GF-UCT180 Ultrasound Gastrovideoscope - Product Usage: These...

The Issue: The adhesive used in the repair of the endoscope was incorrectly prepared....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Roche Diagnostics Corporation

Recalled Item: Anti-HAV IgM test System Recalled by Roche Diagnostics Corporation Due to...

The Issue: Potential for erroneous result messages for the Anti-HAV IgM assay when run...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2018· Meridian Bioscience Inc

Recalled Item: PREMIER Cryptococcal Antigen Recalled by Meridian Bioscience Inc Due to An...

The Issue: An enzyme reagent included in the kit is not maintaining stability through...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2018· Roche Diagnostics Corporation

Recalled Item: COBAS INTEGRA 400 plus analyzer used in the following assays: Recalled by...

The Issue: COBAS INTEGRA¿ 400 plus and cobas c 111 analyzers Additional Extra Wash...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 14, 2018· Roche Diagnostics Corporation

Recalled Item: cobas c 111 with ISE analyzers analyzer used in the Recalled by Roche...

The Issue: COBAS INTEGRA¿ 400 plus and cobas c 111 analyzers Additional Extra Wash...

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

Class II — Potential Health HazardOngoing