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 76417660 of 28,688 recalls

Medical DeviceAugust 30, 2022· Philips Medical Systems (Cleveland) Inc

Recalled Item: Pinnacle3 Radiation Therapy Planning System Recalled by Philips Medical...

The Issue: When computing a radiation dose in the system, the exported dose information...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2022· TELEFLEX LLC

Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...

The Issue: Incidents of device splitting or detaching during use

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 29, 2022· TELEFLEX LLC

Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...

The Issue: Incidents of device splitting or detaching during use

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 29, 2022· TELEFLEX LLC

Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...

The Issue: Incidents of device splitting or detaching during use

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 29, 2022· TELEFLEX LLC

Recalled Item: Filter + Catheter Mount Recalled by TELEFLEX LLC Due to Incidents of device...

The Issue: Incidents of device splitting or detaching during use

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 29, 2022· TELEFLEX LLC

Recalled Item: Iso-Gard Filter S Recalled by TELEFLEX LLC Due to Incidents of device...

The Issue: Incidents of device splitting or detaching during use

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 29, 2022· TELEFLEX LLC

Recalled Item: Iso-Gard Filter S with Expandi-Flex/Elbow: a) Recalled by TELEFLEX LLC Due...

The Issue: Incidents of device splitting or detaching during use

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 29, 2022· Ossur Americas

Recalled Item: OSSUR Power Knee OSSUR Power Knee Recalled by Ossur Americas Due to Battery...

The Issue: Battery may dislodge from the Power Knee

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2022· Leica Microsystems, Inc.

Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....

The Issue: During internal testing, Leica Microsystems has become aware of a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2022· Leica Microsystems, Inc.

Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....

The Issue: During internal testing, Leica Microsystems has become aware of a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2022· Leica Microsystems, Inc.

Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....

The Issue: During internal testing, Leica Microsystems has become aware of a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2022· Leica Microsystems, Inc.

Recalled Item: Leica Surgical Operating Microscopes Recalled by Leica Microsystems, Inc....

The Issue: During internal testing, Leica Microsystems has become aware of a component...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2022· Zimmer, Inc.

Recalled Item: G7 Acetabular System Recalled by Zimmer, Inc. Due to The outer sterile...

The Issue: The outer sterile package cavity has a corner wall thickness that is below...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista High Density Lipoprotein Cholesterol (HDLC) Flex reagent...

The Issue: Dimension Vista¿ High Density Lipoprotein Cholesterol (HDLC) Potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2022· SenTec AG

Recalled Item: sentec 24 / MARe-SF Multi-Site Attachment Ring Easy Recalled by SenTec AG...

The Issue: Weak skin adhesion.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Magnesium (MG) Flex reagent cartridge Siemens Material Number...

The Issue: Dimension Magnesium (MG) Flex reagent cartridge lots may exhibit imprecision...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 17, 2022· Associates of Cape Cod, Inc.

Recalled Item: Fungitell STAT- IVD Assay for (1 ¿ 3)-~-D-Glucan in Serum Recalled by...

The Issue: Incorrect information on the Fungitell STAT clamshells containing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· ConvaTec, Inc

Recalled Item: ConvaTec Active Life Recalled by ConvaTec, Inc Due to impaired functionality...

The Issue: impaired functionality of the release liner

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· ConvaTec, Inc

Recalled Item: ConvaTec Esteem+ Durahesive Plus Recalled by ConvaTec, Inc Due to impaired...

The Issue: impaired functionality of the release liner

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2022· ConvaTec, Inc

Recalled Item: ConvaTec Esteem+ Durahesive Plus Recalled by ConvaTec, Inc Due to impaired...

The Issue: impaired functionality of the release liner

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

Class II — Potential Health HazardOngoing