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. 928 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
928 in last 12 months

Showing 47841–47860 of 51,854 recalls

Medical DeviceMay 28, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...

The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...

The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Medtronic Sofamor Danek USA Inc

Recalled Item: INFUSE(R) Bone Graft Recalled by Medtronic Sofamor Danek USA Inc Due to Kits...

The Issue: Kits contain a collagen sponge recalled by Integra due to possible elevated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2013· Bard Peripheral Vascular Inc

Recalled Item: BARD PERIPHERAL VASCULAR VACCESS¿ PTA Balloon Dilatation Catheters Recalled...

The Issue: Bard Peripheral Vascular (BPV) has confirmed that some product code/lot...

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

Class II — Potential Health HazardOngoing
DrugMay 27, 2013· Earthlabs, Inc. DBA Wise Woman Herbals

Recalled Item: Eyebright Concentrate Topical Eye Rinse Recalled by Earthlabs, Inc. DBA Wise...

The Issue: Lack of Assurance of Sterility; Lack of Assurance of Sterility; product not...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2013· Fresenius Kabi USA, LLC

Recalled Item: Magnesium Sulfate Injection Recalled by Fresenius Kabi USA, LLC Due to...

The Issue: Presence of Particulate Matter: Glass particulate matter was observed in a...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugMay 25, 2013· Hospira Inc.

Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter; single visible particulate was identified...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 24, 2013· SpineFrontier, Inc.

Recalled Item: S-LIFT Inserter Outer Sleeve Product Usage: The Inserter Sleeve is Recalled...

The Issue: The outer sleeve would not fit over the S-LIFT Inserter assembly because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2013· International Biomedical, Ltd.

Recalled Item: VIA Medical Collection Bag Recalled by International Biomedical, Ltd. Due to...

The Issue: International Biomedical has received reports of interference between the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius Service Replacement 0-Ring. Used in as a service part Recalled by...

The Issue: Incorrect rubber nitrile O-rings distributed instead of the correct material...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2013· Gyrus Acmi, Incorporated

Recalled Item: GYRUS ACMI Recalled by Gyrus Acmi, Incorporated Due to lack of sterility...

The Issue: lack of sterility assurance

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2013· Fenwal Inc

Recalled Item: AMICUS Exchange Kit Recalled by Fenwal Inc Due to Fenwal has initiated a...

The Issue: Fenwal has initiated a voluntary Urgent Product Recall for lot FA12C07070 of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-810-000 T4 Zipper Toga (S/M) Sterile Recalled by...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-770-000 T4 Toga Recalled by Stryker Instruments...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Abbott Medical Optics, Inc.

Recalled Item: Sovereign¿ Compact Phacoemulsification System Recalled by Abbott Medical...

The Issue: Abbott Medical Optics Inc. (AMO) initiated this Urgent Notice of Medical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-850-000 T4 Toga Recalled by Stryker Instruments...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Prism Medical Services USA

Recalled Item: BC Hammock Mesh Sling (Large) Recalled by Prism Medical Services USA Due to...

The Issue: The product does not meet the firm's size standards, the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Instruments 0400-720-000S5 T5 Pullover Toga w/Peel Away Recalled by...

The Issue: Based on an accelerated aging test for this product packaging, there is an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Zimmer, Inc.

Recalled Item: Bigliani/Flatow¿ The Complete Solution Fukuda Retractors Small Nonsterile...

The Issue: This is a recall expansion from the 2010 recall which now includes seven...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2013· Prism Medical Services USA

Recalled Item: BC Hammock Mesh Sling (Junior) Recalled by Prism Medical Services USA Due to...

The Issue: The product does not meet the firm's size standards, the product was...

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

Class II — Potential Health HazardOngoing