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 16341–16360 of 51,854 recalls

Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2021· Philips North America Llc

Recalled Item: Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option Recalled by...

The Issue: Significant wear of the Monitor Bracket Assembly shaft goes unrecognized...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2021· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Synapse Cardiovascular (Synapse CV). Software Versions: 6.0 to 6.2.1 The...

The Issue: Software versions 6.0.4 to 6.2.1 using Advanced Reporting -possibility that...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2021· Nico Corp.

Recalled Item: Myriad-LX Light Source-for delivery of light to the surgical field Recalled...

The Issue: (1) Updated IFU for the LX Illumination Packs: Warning - Avoid contact...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2021· Nico Corp.

Recalled Item: NICO Myriad-LX Illumination Pack: Mvriad-LX Illumination Pack. 11ga Recalled...

The Issue: (1) Updated IFU for the LX Illumination Packs: Warning - Avoid contact...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2021· Sentinel CH SpA

Recalled Item: ACE Control Set - IVD Control set for the quantitative Recalled by Sentinel...

The Issue: Claim for stability after reconstitution from lyophilized to liquid form...

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

Class III — Low RiskOngoing
FoodApril 30, 2021· Nutralliance Inc

Recalled Item: Medium Chain Triglyceride (MCT) Powder 70% from Coconut / CocoTrim Recalled...

The Issue: Ingredient tested positive for milk allergen.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 30, 2021· Nutralliance Inc

Recalled Item: Medium Chain Triglyceride (MCT) Powder 50% from Coconut / CocoTrim Recalled...

The Issue: Ingredient tested positive for milk allergen.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodApril 29, 2021· Pepsico Inc

Recalled Item: Evolve Vanilla Bean Plant-Based Protein Shake Recalled by Pepsico Inc Due to...

The Issue: undeclared soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodApril 29, 2021· Pepsico Inc

Recalled Item: Evolve Double Chocolate Plant-Based Protein Shake Recalled by Pepsico Inc...

The Issue: undeclared soy

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic CB10R55R5 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic CB10R79R6 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic 1A46R11 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Covidien, LP

Recalled Item: Adult-Pediatric Electrostatic Filter HME Recalled by Covidien, LP Due to The...

The Issue: The company was notified by their supplier of sterilization services for...

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

Class II — Potential Health HazardOngoing