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. 2,794 recalls have been distributed to North Carolina in the last 12 months.
Showing 6701–6720 of 29,737 recalls
Recalled Item: GEM NEUROTUBE Recalled by Baxter Healthcare Corporation Due to The product...
The Issue: The product is brittle and potentially crumbling upon handling or when being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JOURNEY II UNI XLPE TIBIA INSERT MEDIAL SZ 7-8 8MM Recalled by Smith &...
The Issue: A mispack occurred during the manufacturing process, resulting in the box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEX. BIOPSY FORCEPS 5FR WL 550MM Recalled by Richard Wolf GmbH Due to...
The Issue: Potentially unable to open forceps jaws when the endoscope shaft is bent by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEX. GRASP. FORCEPS 5FR WL 550MM Recalled by Richard Wolf GmbH Due to...
The Issue: Potentially unable to open forceps jaws when the endoscope shaft is bent by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEX. GRASP. FORCEPS 6.6FR WL 550MM Recalled by Richard Wolf GmbH Due to...
The Issue: Potentially unable to open forceps jaws when the endoscope shaft is bent by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEX. GRASP. FORCEPS 5FR WL 550MM Recalled by Richard Wolf GmbH Due to...
The Issue: Potentially unable to open forceps jaws when the endoscope shaft is bent by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff Recalled by...
The Issue: A manufacturing error, resulted in a less than specified diameter of adult...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WALGREENS BANDAGES Recalled by ASO LLC Due to The adhesive bandage contains...
The Issue: The adhesive bandage contains 0.1% benzalkonium chloride impregnated in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA Compact Automated Multi-Parametric Analyzer Recalled by Diagnostica...
The Issue: An internal investigation identified a bug in this firmware version,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA Compact Max fully automatic clinical analyzer Recalled by Diagnostica...
The Issue: An internal investigation identified a bug in this firmware version,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA R Max fully automatic clinical instrument designed to perform Recalled...
The Issue: An internal investigation identified a bug in this firmware version,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile surgical convenience kit: regard Item Number 800706005 Recalled by...
The Issue: The recalling firm was notified by their supplier that the light handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile surgical convenience kit: regard Item Number: 800753005 Recalled by...
The Issue: The recalling firm was notified by their supplier that the light handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile surgical convenience kit: regard Item Number: 880393003 Recalled by...
The Issue: The recalling firm was notified by their supplier that the light handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaOne Reusable Positioning Cannula 11mm Standard Recalled by Covidien LP...
The Issue: There is a manufacturing non-conformance that may result in a metal shaving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 880353009 Recalled...
The Issue: The recalling firm was notified by their supplier that the light handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 880473001 Recalled...
The Issue: The recalling firm was notified by their supplier that the light handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 800756005 Recalled...
The Issue: The recalling firm was notified by their supplier that the light handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile surgical convenience kits: 1. regard Item Number: 880405003 Recalled...
The Issue: The recalling firm was notified by their supplier that the light handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile surgical convenience kit: regard Item Number: 800718003 Recalled by...
The Issue: The recalling firm was notified by their supplier that the light handle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.