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. 1,085 recalls have been distributed to North Carolina in the last 12 months.
Showing 14621–14640 of 54,363 recalls
Recalled Item: Arcos Modular Revision Hip System Recalled by Biomet, Inc. Due to The...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Mini Humeral Stem Recalled by Biomet, Inc. Due...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NavitrackER Kit A: Knee Recalled by Orthosoft, Inc. dba Zimmer CAS Due to...
The Issue: The product was released for distribution without passing sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Mini Humeral Stem Recalled by Biomet, Inc. Due...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Mini Humeral Stem Recalled by Biomet, Inc. Due...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Primary Shoulder Stem Recalled by Biomet, Inc....
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Primary Shoulder Stem Recalled by Biomet, Inc....
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Mini Humeral Stem Recalled by Biomet, Inc. Due...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Primary Shoulder Stem Recalled by Biomet, Inc....
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Luer Lok Access Device - intended as a sterile Recalled by...
The Issue: May shed contaminant particles into the urine specimen that may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXCERA BASE -a Dental resins for the fabrication of artificial teeth...
The Issue: Manufactured in a non-FDA-registered manufacturing facility and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXCERA SMILE -a Dental resins for the fabrication of artificial teeth...
The Issue: Manufactured in a non-FDA-registered manufacturing facility and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition X (Product Number 781356) - HA FlexTrak II Recalled by...
The Issue: Magnetic materials were used for the wheels of trolley. Wheels with magnetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T (Product Number 781396) - HA FlexTrak II (Accessory Recalled by...
The Issue: Magnetic materials were used for the wheels of trolley. Wheels with magnetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition X (Product Number 781358) - HA FlexTrak II Recalled by...
The Issue: Magnetic materials were used for the wheels of trolley. Wheels with magnetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dole 10oz Very Veggie SKU: 532 Recalled by Dole Fresh Vegetables Inc Due to...
The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Kroger 12 oz American Blend SKU: 3003 Recalled by Dole Fresh Vegetables Inc...
The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dole 10 oz Very Veggie / Ranache de Legumes SKU: 2684 Recalled by Dole Fresh...
The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dole 13oz Southwest Kit SKU: 2776 Recalled by Dole Fresh Vegetables Inc Due...
The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dole 11 oz Greener Selection / Selection de Verdure Recalled by Dole Fresh...
The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...
Recommended Action: Do not consume. Return to store for a refund or discard.