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. 1,824 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,824 in last 12 months

Showing 3986139880 of 54,363 recalls

Medical DeviceAugust 14, 2015· Limacorporate S.p.A

Recalled Item: SMR Shoulder/Spalla Trial Humeral Head diameter .42 mm Recalled by...

The Issue: The dimensions of the mating features of the recalled products are out of...

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

Class II — Potential Health HazardOngoing
DrugAugust 13, 2015· GlaxoSmithKline, LLC.

Recalled Item: Bactroban Ointment (mupirocin calcium) Recalled by GlaxoSmithKline, LLC. Due...

The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· GlaxoSmithKline, LLC.

Recalled Item: Bactroban Cream (mupirocin calcium) Recalled by GlaxoSmithKline, LLC. Due to...

The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· GlaxoSmithKline, LLC.

Recalled Item: Mupirocin Calcium Cream Recalled by GlaxoSmithKline, LLC. Due to Penicillin...

The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· Dr. Reddy's Laboratories, Inc.

Recalled Item: Amlodipine besylate and Atorvastatin calcium Tablets Recalled by Dr. Reddy's...

The Issue: Subpotent Drug: Subpotent atorvastatin.

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

Class III — Low RiskOngoing
Refund
DrugAugust 13, 2015· GlaxoSmithKline, LLC.

Recalled Item: Bactroban (mupirocin calcium) Nasal Ointment Recalled by GlaxoSmithKline,...

The Issue: Penicillin Cross Contamination and Presence of Foreign Substance. Product...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 11, 2015· Zimmer, Inc.

Recalled Item: Zimmer Universal Locking System Recalled by Zimmer, Inc. Due to It was found...

The Issue: It was found through review of open Complaints and stock investigations that...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2015· Synthes (USA) Products LLC

Recalled Item: Dynamic Locking Screw System (DLS) 3.7mm & Dynamic Locking Screw (DLS) 5.0mm...

The Issue: DLS pin breakage during planned implant removal, after uneventful and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2015· GE Healthcare

Recalled Item: Centricity Universal Viewer Product Usage: The Centricity Universal Viewer...

The Issue: Images from the Centricity PACS-IW with Universal Viewer and Centricity...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2015· Alcon Research, Ltd.

Recalled Item: LX3 Floor Stand for Endure Luxite Envision Optical System Recalled by Alcon...

The Issue: Alcon is initiating a voluntary recall of all LX3 Microscope Floor Stands...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2015· GE Healthcare

Recalled Item: Centricity PACS-IW with Universal Viewer Product Usage: The Centricity...

The Issue: Images from the Centricity PACS-IW with Universal Viewer and Centricity...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2015· Biomet 3i, LLC

Recalled Item: Biomet 3i Narrow Right Angle Large Driver Tip (Hexed). Driver Recalled by...

The Issue: The RASH3N, a hexed, abutment screw driver tip has been labeled and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2015· Biomet 3i, LLC

Recalled Item: Biomet 3i Narrow Right Angle Square Driver Tip. Driver tips Recalled by...

The Issue: RASQ3N, a square, abutment screw driver tip has been labeled and distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Crocodile Grasper Recalled by Intuitive Surgical, Inc. Due to In certain...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing