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. 2,701 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,701 in last 12 months

Showing 95419560 of 28,688 recalls

Medical DeviceMay 27, 2021· Cell Marque Corporation

Recalled Item: Cell Marque Antibodies Recalled by Cell Marque Corporation Due to Product...

The Issue: Product distributed for use as an In-vitro Diagnostics without FDA clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2021· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: 3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60...

The Issue: Telepack may not power on when using the 3AA battery cradle.

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

Class III — Low RiskOngoing
Medical DeviceMay 27, 2021· Cell Marque Corporation

Recalled Item: Cell Marque Recalled by Cell Marque Corporation Due to Product distributed...

The Issue: Product distributed for use as an In-vitro Diagnostics without FDA clearance

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS pheno- angiography systems developed for single and biplane diagnostic...

The Issue: Software error VE10B -In case of a fault within the drivetrain of an axis...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion systems with software release R1.x Recalled by PHILIPS MEDICAL...

The Issue: In the Azurion system, the user can add a new study to a patient by...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Philips Healthcare

Recalled Item: Azurion systems with software release R2.0.x Recalled by Philips Healthcare...

The Issue: In the Azurion system, the user can add a new study to a patient by...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Owen Mumford USA, Inc.

Recalled Item: Unifine Pentips Plus Recalled by Owen Mumford USA, Inc. Due to Mixed Up. Two...

The Issue: Mixed Up. Two (2) cases of Unifine Pentips Plus 4mm pen needles have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Flowonix Medical Inc

Recalled Item: Physician Order Form (PL-15400-00 Recalled by Flowonix Medical Inc Due to...

The Issue: Physician Order Form (PL-15400-00 Nov 2018) distributed is discontinued due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2021· Medline Industries Inc

Recalled Item: Cotton Rounds/Pads under the following brand names: 1. BEAUTY 360 Recalled...

The Issue: Potential for mold contamination (Aspergillus vadensis)

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2021· Remote Diagnostic Technologies Ltd.

Recalled Item: Tempus Pro - Patient physiological monitor Recalled by Remote Diagnostic...

The Issue: The Tempus Pro (Trizeps 7 only) when used in combination with a specified...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· GE Healthcare, LLC

Recalled Item: CARESCAPE PDM-Masimo SpO2. Physiological data monitor. Recalled by GE...

The Issue: Masimo SpO2 Saturation Values can become frozen after an extended length of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Canon Medical System, USA, INC.

Recalled Item: Canon Vantage Titan 3T Recalled by Canon Medical System, USA, INC. Due to...

The Issue: The MRI system contains a component that does not meet the appropriate flame...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Canon Medical System, USA, INC.

Recalled Item: Toshiba Vantage Tiitan 1.5T with Standard gradient Recalled by Canon Medical...

The Issue: The MRI system contains a component that does not meet the appropriate flame...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Canon Medical System, USA, INC.

Recalled Item: Canon Vantage Tiitan 1.5T Recalled by Canon Medical System, USA, INC. Due to...

The Issue: The MRI system contains a component that does not meet the appropriate flame...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Canon Medical System, USA, INC.

Recalled Item: Canon Vantage Galan 3T Recalled by Canon Medical System, USA, INC. Due to...

The Issue: The MRI system contains a component that does not meet the appropriate flame...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Nonsterile Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Sterile Cesarean Birth Drape with Dual Layer Anesthesia Screen Recalled by...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Sterile Femoral Angiography Drape with Single Pouch Recalled by Cardinal...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Nonsterile Femoral Angiography Drape Recalled by Cardinal Health 200, LLC...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Nonsterile Femoral Angiography Drape with Single Pouch Recalled by Cardinal...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing