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. 2,529 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,529 in last 12 months

Showing 2698127000 of 28,688 recalls

Medical DeviceFebruary 1, 2013· ICU

Recalled Item: The Plum A+ Infusion Systems are a multipurpose family of Recalled by ICU...

The Issue: A possible interruption of therapy when an E321 error code occurs while...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Orthofix, Inc

Recalled Item: Firebird Spinal Fixation System Recalled by Orthofix, Inc Due to There is a...

The Issue: There is a possibility that the Set Screw (p/n 90-2923) sub-component of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Greiner Bio-One North America, Inc.

Recalled Item: VACUETTE Safety Blood Collection Set + Luer Adapter Recalled by Greiner...

The Issue: The VACUETTE Safety Blood Collection Set + Luer Adapter may display leaking...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Exactech, Inc.

Recalled Item: Optetrak Logic Comprehensive Knee Prosthesis System Recalled by Exactech,...

The Issue: A dimensional mismatch was identified which can potentially allow for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+3 Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Hallu-Fix cannulated screw driver (model number P/N 129733ND) and...

The Issue: The firm has received numerous complaints of the cannulated screw driver tip...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Hyperbaric Infusion System is a cassette based Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+3 Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2013· Hospira Inc.

Recalled Item: The Plum A+3 Infusion System is a cassette based multifunction Recalled by...

The Issue: Plum A+ infusers have the potential for the distal (occlusion) press sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2013· Hitachi Medical Systems America Inc

Recalled Item: Echelon Recalled by Hitachi Medical Systems America Inc Due to Hitachi...

The Issue: Hitachi discovered a software error that can occur when simultaneously...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens AXIOM Artis zee/zeego systems equipped with generator A100 Plus...

The Issue: During the course of product monitoring, Siemens became aware of a tolerance...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 31, 2013· Medtronic Navigation, Inc.

Recalled Item: Medtronic O-arm Imaging System Product Usage: image-intensified fluoroscopic...

The Issue: Potential failure of the braking system that controls the O-arm Imaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2013· Edwards Lifesciences, LLC

Recalled Item: Pressure Monitoring sets with VAMP Plus closed blood sampling system...

The Issue: The device is being recalled because the firm has received multiple...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2013· QIAGEN Gaithersburg, Inc.

Recalled Item: QIAGEN artus CMV RG PCR ASR (96) (Catalog number 4503225) Recalled by QIAGEN...

The Issue: CMV RG PCR kits may contain a mixture of incorrect vials among the correct...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 30, 2013· QIAGEN Gaithersburg, Inc.

Recalled Item: QIAGEN artus CMV RG PCR ASR (24) (Catalog number 4503223) Recalled by QIAGEN...

The Issue: CMV RG PCR kits may contain a mixture of incorrect vials among the correct...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 29, 2013· Vascular Solutions, Inc.

Recalled Item: Vascular Solutions Recalled by Vascular Solutions, Inc. Due to Vascular...

The Issue: Vascular Solutions, Inc has discovered a potential problem with a number of...

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

Class II — Potential Health HazardOngoing