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. 1,126 recalls have been distributed to North Carolina in the last 12 months.
Showing 4781–4800 of 29,737 recalls
Recalled Item: TFNA Femoral Nail 11mm Recalled by Synthes (USA) Products LLC Due to...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RIA Tube Assembly Recalled by Synthes (USA) Products LLC Due to Products not...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: impression coping Recalled by Thommen Medical AG Due to The depth of the...
The Issue: The depth of the internal canal was not manufactured according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Erythropoietin (EPO) Assay (100 Test) Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed an average negative bias of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5MM Drill Bit/QC/85MM Sterile-surgical Recalled by Synthes (USA) Products...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TFNA Femoral Nail 9mm Recalled by Synthes (USA) Products LLC Due to Products...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Opal Recalled by Synthes (USA) Products LLC Due to Products not sterilized,...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDSORB IPS Battery Pack Recalled by Synthes (USA) Products LLC Due to...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5MM DRILL BIT/QC/GOLD/110MM STERILE-surgical Recalled by Synthes (USA)...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13 mm Titanium Hindfoot Arthrodesis Cannulated Nails EX Recalled by Synthes...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VA-LCP Clavicle Plate 2.7 Recalled by Synthes (USA) Products LLC Due to...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVS Health Waterproof Wound Tracking Dressing Recalled by MEDLINE...
The Issue: Product failed sterility testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stay-safe /Luer Lock Adapter 4 in Recalled by Fresenius Medical Care...
The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stay-safe /Luer Lock Catheter Ext. 18 in Recalled by Fresenius Medical Care...
The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stay-safe /Luer Catheter Ext. 6 in Recalled by Fresenius Medical Care...
The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stay-safe /Luer Lock Catheter Ext. 12 in Recalled by Fresenius Medical Care...
The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stay-safe /Safe Lock Catheter Ext. 12 in Recalled by Fresenius Medical Care...
The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head Recalled by...
The Issue: Mislabeled: Packaging incorrectly a MobileLink Dual Mobility insert type F...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tensive Conductive Adhesive Gel Recalled by Parker Laboratories, Inc. Due to...
The Issue: Five complaints were received related to viscosity of Tensive Conductive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Duet External Drainage and Monitoring System Recalled by Medtronic...
The Issue: Potential for catheter disconnection from the patient line stopcock connectors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.