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. 1,748 recalls have been distributed to North Carolina in the last 12 months.
Showing 46861–46880 of 54,363 recalls
Recalled Item: Medtronic neurostimulators. Restore (37711) Recalled by Medtronic...
The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Neuromodulation Due to Medtronic...
The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-10" Hemoglobin Testing System Recalled by Bio-Rad Laboratories, Inc. Due...
The Issue: On a rare occasion the D-10 software might generate an extra result by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPort Slim Implantable Port Recalled by Bard Access Systems Due to...
The Issue: Labeling discrepancy.The label states that the implantable port contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advil PM Caplets Recalled by Pfizer Us Pharmaceutical Group Due to Subpotent...
The Issue: Subpotent Drug: This lot is being recalled because of out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Laura Lynn French Onion Recalled by Durrset Amigos, Ltd. Due to Undeclared Wheat
The Issue: Undeclared Wheat due to a supplier's inadvertent use of a wheat product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Roundy's Salsa Con Queso Recalled by Durrset Amigos, Ltd. Due to Undeclared...
The Issue: Undeclared Wheat due to a supplier's inadvertent use of a wheat product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HY-TOP FRENCH ONION DIP Recalled by Durrset Amigos, Ltd. Due to Undeclared Wheat
The Issue: Undeclared Wheat due to a supplier's inadvertent use of a wheat product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: H-E-B Chipotle Con Queso Recalled by Durrset Amigos, Ltd. Due to Undeclared...
The Issue: Undeclared Wheat due to a supplier's inadvertent use of a wheat product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HILL COUNTRY FARE Recalled by Durrset Amigos, Ltd. Due to Undeclared Wheat
The Issue: Undeclared Wheat due to a supplier's inadvertent use of a wheat product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: my essentials brand sour cream Recalled by HP Hood LLC Due to Foreign Object...
The Issue: HP Hood LLC received one complaint of a foreign object in sour cream product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Novocastra Liquid Mouse Monoclonal Antibody Glutathione S-Transferase pi...
The Issue: Novocastra Liquid Mouse Monoclonal Antibody Glutathione S-Transferase pi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part 475630 Recalled by Biomet, Inc. Due to Incorrect labeling on specific...
The Issue: Incorrect labeling on specific lots of the Intramedullary Bone Saw. The Saw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part 475620 Intramedullary Bone Saw CAM Assembly Size 12mm Recalled by...
The Issue: Incorrect labeling on specific lots of the Intramedullary Bone Saw.The Saw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part 475625 Recalled by Biomet, Inc. Due to Incorrect labeling on specific...
The Issue: Incorrect labeling on specific lots of the Intramedullary Bone Saw. The Saw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿/Apollo" Knee: M/B PAT SZ0 NATURAL-KNEE M/B PAT SZ1...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ II Posterior Stabilized (P.S.) Condylar Tibial Inserts: N-K II...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ II - Unicompartmental Knee Prosthesis: CONG TIB INS SZ1/2...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo Knee Tibial Baseplate/Knee Tibial Insert: CONG TIB INS SZ0/19MM...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ N-K II DOMED ALL-POLY PAT Recalled by Zimmer, Inc. Due to A...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.