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. 2,572 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
2,572 in last 12 months

Showing 1888118900 of 28,688 recalls

Medical DeviceFebruary 27, 2017· LIEBEL-FLARSHEIM COMPANY LLC

Recalled Item: Liebel-Flarsheim Direct Digital Imaging System (DDIS) Liebel-Flarsheim...

The Issue: Software issue. The difference between the display and dosimeter readings In...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2017· Philips North America, LLC

Recalled Item: HeartStart MRx Monitor/Defibrillator Recalled by Philips North America, LLC...

The Issue: HeartStart MRx Monitor/Defibrillator may may exhibit abnormal behavior when...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 23, 2017· Streck

Recalled Item: Cyto-Chex BCT - blood specimen collection device - Immunophenotyping...

The Issue: Complaints of the 2.0ml tube stopper coming loose during phlebotomy when...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Enzyme 2 Calibrator Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has confirmed a positive bias of up to 41% in...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 23, 2017· Hill-Rom, Inc.

Recalled Item: TotalCare Bed Systems Recalled by Hill-Rom, Inc. Due to The bed exit alarm...

The Issue: The bed exit alarm may not function properly if the alarm has been armed for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: ILLINOIS (TJ) NEEDLE ASPIRATION [15GA Recalled by Carefusion 2200 Inc Due to...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: JAMSHIDI NEEDLE BIOPSY [15G X 100MM DISP Recalled by Carefusion 2200 Inc Due...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: JAMSHIDI (TJ) NEEDLE BONE MARROW [a.) 13G x 3.5 Recalled by Carefusion 2200...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: Manometer Recalled by Carefusion 2200 Inc Due to The integrity of the...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: Thoracentesis/ Paracentesis Kit 10/CS Recalled by Carefusion 2200 Inc Due to...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2017· Carefusion 2200 Inc

Recalled Item: JAMSHIDI (TJ) NEEDLE BM ASP MAC [a.) 13G x 3.5 Recalled by Carefusion 2200...

The Issue: The integrity of the sterile packaging is potentially compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2017· Ace Surgical Supply Co., Inc.

Recalled Item: INFINITY Internal Hex Healing Abutment Recalled by Ace Surgical Supply Co.,...

The Issue: Incorrect device was packaged.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Orthosoft, Inc. dba Zimmer CAS

Recalled Item: SmartTools Knee System Orthopedic Stereotaxic Instrument Recalled by...

The Issue: There has been an increase in the number of complaints regarding bent or...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· CareFusion 303, Inc.

Recalled Item: MaxGuard Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion is...

The Issue: CareFusion is recalling the MaxGuard Extension Set due to reports of leaks...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph 6 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: The mobile-specific instructions was not shipped to a limited population of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph 16 TruePoint TrueV - 4R Recalled by Siemens Medical Solutions USA...

The Issue: The mobile-specific instructions was not shipped to a limited population of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph 6 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: The mobile-specific instructions was not shipped to a limited population of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Signal Medical Corporation

Recalled Item: Soft Face "No Bounce" Mallet Model/Catalog: BIO-1-1090 Recalled by Signal...

The Issue: Potential for poly tip of the mallet to come off during use. Potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1-Level Sensor II Gel Pads Product Recalled...

The Issue: Terumo CVS initiated a voluntary recall for the Level Sensor II Pads and...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1-Level Sensor II Pads Recalled by Terumo...

The Issue: Terumo CVS initiated a voluntary recall for the Level Sensor II Pads and...

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

Class II — Potential Health HazardOngoing