Product Recalls in North Carolina

Product recalls affecting North Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to North Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,900 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,900 in last 12 months

Showing 2754127560 of 54,363 recalls

Medical DeviceJuly 12, 2018· Orthosensor, Inc.

Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Right Recalled...

The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Ultradent Products, Inc.

Recalled Item: Enamelast Cool Mint/OT Varnish 5% NaF Mint Label Enamelast Unit Recalled by...

The Issue: Dental varnish has the possibility of having an unpleasant and off flavor.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Medical Components, Inc dba MedComp

Recalled Item: Duo-Flow XTP Straight Full Set Recalled by Medical Components, Inc dba...

The Issue: The suture wings have the potential to crack or break. Potential patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Immunodiagnostic Products - FSH Reagent Pack (10758750000302) 1931922...

The Issue: The recalling firm determined that biased results may occur for specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Orthosensor, Inc.

Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Left Recalled by...

The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Orthosensor, Inc.

Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Right Recalled...

The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Immunodiagnostic Products - Prolactin Reagent Pack (10758750000111)...

The Issue: The recalling firm determined that biased results may occur for specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Orthosensor, Inc.

Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Right Recalled by...

The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Orthosensor, Inc.

Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Left Recalled by...

The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Orthosensor, Inc.

Recalled Item: OrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Left Recalled by...

The Issue: Some sensors were reported to have fluid inside the posterior lateral corner...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Medical Components, Inc dba MedComp

Recalled Item: SOFT-LINE DUO-FLOW DOUBLE LUMEN CATHETER/CATHETER SET Recalled by Medical...

The Issue: The suture wings have the potential to crack or break. Potential patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2018· Medical Components, Inc dba MedComp

Recalled Item: Duo-Flow Double Lumen Catheter Only/Catheter Set Recalled by Medical...

The Issue: The suture wings have the potential to crack or break. Potential patient...

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

Class II — Potential Health HazardOngoing
DrugJuly 12, 2018· Sun Pharmaceutical Industries, Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by Sun Pharmaceutical Industries,...

The Issue: Presence of Particulate Matter: organic and inorganic compounds detected in...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 12, 2018· The Pictsweet Company

Recalled Item: Pictsweet Farms Steam'ables Baby Brussels Sprouts***NET WT 12 OZ...

The Issue: Undeclared allergens on the labeling.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 11, 2018· Spacelabs Healthcare, Ltd.

Recalled Item: Arkon Anesthesia Delivery System with Arkon Software Version 2.70 Recalled...

The Issue: Arkon Anesthesia Delivery System may go into a failed state (mechanical...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: 400mL Recalled by COVIDIEN LLC Due to The temperature sensor catheters may...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: P400 PREM U/M 16FR TMPSNS Recalled by COVIDIEN LLC Due to The temperature...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides failed to meet current claims for Limit of Blank (LoB), Limit of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products CREA Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides did not meet the current claims for Limit of Blank (LoB), Limit...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: 400mL Recalled by COVIDIEN LLC Due to The temperature sensor catheters may...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing