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. 1,117 recalls have been distributed to North Carolina in the last 12 months.
Showing 10501–10520 of 29,737 recalls
Recalled Item: ChemoPlus Drug Spill Kit-INSTI Recalled by Cardinal Health 200, LLC Due to...
The Issue: Gowns included in the kits potentially have rips, holes, tears, incomplete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lab Coats SMS Medium White Recalled by Cardinal Health 200, LLC Due to...
The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gown Kendall Blue L Recalled by Cardinal Health 200, LLC Due to Foreign...
The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The PrisMax System Version II Hemodialysis Delivery System: Automatic...
The Issue: Variability in the performance of the tubing in the ARPS (Automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gown Isolation W/Ties Univ Ylw Recalled by Cardinal Health 200, LLC Due to...
The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lab Coats SMS 2X-Large Blue Recalled by Cardinal Health 200, LLC Due to...
The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gown Isolation W/Ties Univ Blu Recalled by Cardinal Health 200, LLC Due to...
The Issue: There is a potential for rips, holes, tears, incomplete and/or open seams,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infusion Pump Recalled by Baxter Healthcare Corporation Due to Battery...
The Issue: Battery performance issues related to prolonged storage.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9180 Electrolyte Analyzer - Product Usage: intended to be used Recalled by...
The Issue: May display Calcium results on the screen with wrong arrow direction which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow AGB+ Multi-Lumen CVC Kit 7Fr 3 Lumen- Intended for Recalled by Arrow...
The Issue: The lidstock / information card on the kits correctly states the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHILIPS BATTERY Recalled by Respironics California, LLC Due to Due to...
The Issue: Due to unqualified "design verification" batteries being shipped to customers.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cascade Abrazo aPTT Test Card - Product Usage: are to Recalled by Helena...
The Issue: Intermittent potential for shorter than expected clot times.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX UP 2.8MMCH 25G 5MM Recalled by Aomori Olympus Co., Ltd....
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INJECTOR FORCEMAX LOWER 25G 6MM Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SD-210U-10 ELECTROSURGICAL SNARE Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PBD-203-0710 BILIARY STENT Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SD-240U-25 ELECTROSURGICAL SNARE Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NA-200H-8022 22G EZSHOT ASPIRATION NEEDLE Recalled by Aomori Olympus Co.,...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: K-204 GUIDE SHEATH KIT 2.6MM Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: B5-2Q BALLOON CATHETER Recalled by Aomori Olympus Co., Ltd. Due to...
The Issue: Inspection confirmed a small percentage of sterile packages with inadequate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.