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. 993 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
993 in last 12 months

Showing 38101–38120 of 54,363 recalls

Medical DeviceJanuary 11, 2016· Horiba Instruments Inc

Recalled Item: ABX PENTRA Lactic Acid CP ref. A11A01721 reagent is intended Recalled by...

The Issue: N-Acetylcysteine (NAC) present in the blood of patients treated for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew BEAVER Blade 4.0mm Part Number: 72203307 Orthopedic Recalled...

The Issue: Blade exhibiting fracture during hip arthroscopy procedures

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Horiba Instruments Inc

Recalled Item: ABX PENTRA Uric Acid CP ref. A11A01670 is an in Recalled by Horiba...

The Issue: N-Acetylcysteine (NAC) present in the blood of patients treated for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Horiba Instruments Inc

Recalled Item: ABX PENTRA Triglycerides CP ref. A11A01640 is an in vitro Recalled by Horiba...

The Issue: N-Acetylcysteine (NAC) present in the blood of patients treated for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Horiba Instruments Inc

Recalled Item: ABX PENTRA Glucose PAP CP ref. A11A01668 reagent is intended Recalled by...

The Issue: N-Acetylcysteine (NAC) present in the blood of patients treated for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Biomet, Inc.

Recalled Item: LPS-FLEX GSF OPT prosthesis Recalled by Zimmer Biomet, Inc. Due to LDPE bag...

The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Biomet, Inc.

Recalled Item: VERSYS 6 INCH BEADED FC 1 prosthesis Recalled by Zimmer Biomet, Inc. Due to...

The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2016· Zimmer Biomet, Inc.

Recalled Item: Bipolar Shell prosthesis Recalled by Zimmer Biomet, Inc. Due to LDPE bag...

The Issue: LDPE bag containing the implant adheres to the highly polished implant surface.

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

Class II — Potential Health HazardOngoing
DrugJanuary 11, 2016· Pfizer Inc.

Recalled Item: Lyrica (pregabalin) capsules Recalled by Pfizer Inc. Due to FAILED...

The Issue: FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 11, 2016· Pfizer Inc.

Recalled Item: Lyrica (pregabalin) capsules Recalled by Pfizer Inc. Due to FAILED...

The Issue: FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Herb Viagra Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Hard Ten Days Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Bull's Genital Recalled by R Thomas Marketing, LLC Due to Marketed Without...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: African Black Ant Recalled by R Thomas Marketing, LLC Due to Marketed...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Super Hard Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Bigger Longer More Time More Sperms Recalled by R Thomas Marketing, LLC Due...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Germany Niubian Recalled by R Thomas Marketing, LLC Due to Marketed Without...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Black Ant Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Mojo Risen Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2016· R Thomas Marketing, LLC

Recalled Item: Real Skill Recalled by R Thomas Marketing, LLC Due to Marketed Without An...

The Issue: Marketed Without An Approved NDA/ANDA

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

Class I — Serious Health HazardOngoing
Refund