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. 1,064 recalls have been distributed to South Carolina in the last 12 months.

51,854 total recalls
1,064 in last 12 months

Showing 15341–15360 of 28,688 recalls

Medical DeviceAugust 12, 2018· The Binding Site Group, Ltd.

Recalled Item: VaccZyme Human Anti-Haemophilus influenza type b Enzyme Immunoassay Kit For...

The Issue: A deterioration of performance was identified with influenza type B Enzyme...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2018· Medtest Holdings, Inc.

Recalled Item: Pointe Scientific AutoHDL/LDL Cholesterol Calibrator Recalled by Medtest...

The Issue: Vials of the autoHDL/LDL Calibrator were shipped without a vial label.

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

Class III — Low RiskOngoing
Medical DeviceAugust 9, 2018· Biomet UK Ltd.

Recalled Item: HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Recalled...

The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2018· Biomet UK Ltd.

Recalled Item: HipLOC Hip Fracture Fixation System- Hiploc System 130¿ Plate 38 Recalled by...

The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2018· Biomet UK Ltd.

Recalled Item: HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Recalled...

The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2018· Biomet UK Ltd.

Recalled Item: HipLOC Hip Fracture Fixation System-Hiploc System 140¿ Plate 38 mm Recalled...

The Issue: HipLOC System Plate Barrel due to an undersized bore on the HipLOC plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2018· Besmed Health Business Corporation

Recalled Item: Ambu Aura40 Standard Recalled by Besmed Health Business Corporation Due to...

The Issue: Ambu Aura40 Standard, Reusable Laryngeal Mask packaged in a pouch marked...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-P160 Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-3C160 Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Right 125 9 mm x 320 mm Recalled by Zimmer Biomet,...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-1T180 Recalled by Olympus Corporation of the Americas...

The Issue: The attachment of non-Olympus accessories to the bronchoscope s instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 125 11 mm x 360 mm Recalled by Zimmer Biomet,...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Right 125 9 mm x 460 mm Recalled by Zimmer Biomet,...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 125 13 mm x 340 mm Recalled by Zimmer Biomet,...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail 130 11 mm x 180 mm Recalled by Zimmer Biomet, Inc....

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 125 9 mm x 440 mm Recalled by Zimmer Biomet,...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Right 125 13 mm x 440 mm Recalled by Zimmer...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Left 130 11 mm x 360 mm Recalled by Zimmer Biomet,...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Magellan Diagnostics, Inc.

Recalled Item: Magellan LeadCare¿ II Blood Lead Test Kit. In Vitro Test Recalled by...

The Issue: Defect with the calibration button for lot 1808M. Level 1 and Level 2...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2018· Zimmer Biomet, Inc.

Recalled Item: Affixus Hip Fracture Nail Right 130 13 mm x 360 mm Recalled by Zimmer...

The Issue: There were complaints indicating that when the product was opened in...

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

Class II — Potential Health HazardOngoing