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

54,363 total recalls
1,064 in last 12 months

Showing 16661–16680 of 54,363 recalls

Medical DeviceMay 26, 2021· Edwards Lifesciences, LLC

Recalled Item: Edwards TruWave (3 cc)/VAMP Jr 48 in (120 cm) Kit Recalled by Edwards...

The Issue: There is a potential that the pressure tubing may detach from the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Flowonix Medical Inc

Recalled Item: Physician Order Form (PL-15400-00 Recalled by Flowonix Medical Inc Due to...

The Issue: Physician Order Form (PL-15400-00 Nov 2018) distributed is discontinued due...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Edwards Lifesciences, LLC

Recalled Item: Edwards TruWave (30 cc)/VAMP Jr/52 in (132 cm) Kit Recalled by Edwards...

The Issue: There is a potential that the pressure tubing may detach from the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Edwards Lifesciences, LLC

Recalled Item: Edwards TruWave (30 cc)/VAMP Jr Kit Recalled by Edwards Lifesciences, LLC...

The Issue: There is a potential that the pressure tubing may detach from the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Edwards Lifesciences, LLC

Recalled Item: Edwards TruWave (3 cc)/VAMP Jr Recalled by Edwards Lifesciences, LLC Due to...

The Issue: There is a potential that the pressure tubing may detach from the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Edwards Lifesciences, LLC

Recalled Item: Edwards Recalled by Edwards Lifesciences, LLC Due to There is a potential...

The Issue: There is a potential that the pressure tubing may detach from the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Edwards Lifesciences, LLC

Recalled Item: Edwards VAMP Jr. 6 in (15 cm) Recalled by Edwards Lifesciences, LLC Due to...

The Issue: There is a potential that the pressure tubing may detach from the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Edwards Lifesciences, LLC

Recalled Item: Edwards TruWave 3 cc/VAMP Jr Kit Recalled by Edwards Lifesciences, LLC Due...

The Issue: There is a potential that the pressure tubing may detach from the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Owen Mumford USA, Inc.

Recalled Item: Unifine Pentips Plus Recalled by Owen Mumford USA, Inc. Due to Mixed Up. Two...

The Issue: Mixed Up. Two (2) cases of Unifine Pentips Plus 4mm pen needles have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2021· Edwards Lifesciences, LLC

Recalled Item: Edwards TruWave x 2 (3 cc)/VAMP Jr/54 in (136) Kit Recalled by Edwards...

The Issue: There is a potential that the pressure tubing may detach from the blood...

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

Class II — Potential Health HazardOngoing
DrugMay 26, 2021· McKesson Corporation dba McKesson Drug Company

Recalled Item: Levetiracetam Tablets USP Recalled by McKesson Corporation dba McKesson Drug...

The Issue: Labeling; Wrong Barcode; error in the machine-readable barcode which could...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 25, 2021· Remote Diagnostic Technologies Ltd.

Recalled Item: Tempus Pro - Patient physiological monitor Recalled by Remote Diagnostic...

The Issue: The Tempus Pro (Trizeps 7 only) when used in combination with a specified...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2021· Medline Industries Inc

Recalled Item: Cotton Rounds/Pads under the following brand names: 1. BEAUTY 360 Recalled...

The Issue: Potential for mold contamination (Aspergillus vadensis)

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

Class II — Potential Health HazardOngoing
FoodMay 24, 2021· IHERB LLC

Recalled Item: Solumeve Hydrolyzed Collagen Peptides Recalled by IHERB LLC Due to...

The Issue: Informed by contract manufacturer that the MCT ingredient used in their...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 21, 2021· Reser's Fine Foods, Inc.

Recalled Item: ***Chicken Street Taco Kit with Trays Recalled by Reser's Fine Foods, Inc....

The Issue: Undeclared egg. The cup of Chipotle Crema in the Chicken Street Taco kits...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Sterile Femoral Angiography Drape Recalled by Cardinal Health 200, LLC Due...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Nonsterile Radial/Femoral Angiography Drape Recalled by Cardinal Health 200,...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Nonsterile Femoral Angiography Drape with Single Pouch Recalled by Cardinal...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Nonsterile Femoral Angiography Drape Recalled by Cardinal Health 200, LLC...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 21, 2021· Cardinal Health 200, LLC

Recalled Item: Sterile Femoral Angiography Drape with Single Pouch Recalled by Cardinal...

The Issue: The plastic film used to manufacture these Angiography Drape and Cesarean...

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

Class II — Potential Health HazardOngoing