State
72,992 recalls have nationwide distribution and so reach North Carolina. 10,261 additional recalls listed North Carolina specifically in their distribution scope.
Of the 10,261 recalls naming North Carolina we have scored against our rubric, 1,476 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,520 (25%) are Severe.
Which agencies issued them
These figures cover only the 10,261 recalls whose distribution notice names North Carolina specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Boston Scientific's AXIOS Stent Delivery System (47 units affected) is recalled because the outer sheath can detach and prevent proper stent expansion, requiring device exchange.
McKesson is recalling Inflectra (infliximab-dyyb) injectable drug due to manufacturing quality deviations. A batch intended for quarantine was inadvertently distributed to patients nationwide.
Karl Storz ureteroscopes contain reprocessing instructions that have not been reviewed and approved by the FDA. Affected devices should not be reprocessed using unapproved methods.
LivaNova's SenTiva DUO vagus nerve stimulation device may stop delivering therapy due to an internal component issue. The recall affects 84 units distributed worldwide.
Karl Storz ureteroscopes are being recalled because their instructions contain reprocessing procedures that have not been reviewed or approved by the FDA. The recall affects 3,069 units distributed nationwide.
Boston Scientific recalls 1,399 units of AXIOS stent delivery systems due to outer sheath detachment that can prevent proper device expansion, requiring procedure prolongation and device exchange.
Karl Storz Endoscopy is recalling its Pediatric Uretero-Renoscope 7.3 Fr. due to unapproved reprocessing instructions. The device instructions contain procedures not reviewed or approved by the FDA for safety and efficacy.
Duloxetine Delayed-Release Capsules USP 20 mg are being recalled nationwide due to presence of nitrosamine impurity above FDA acceptable limits. No adverse events have been reported.
Karl Storz is recalling 221 cysto-urethroscopes because their reprocessing instructions have not been FDA-approved. Medical facilities should stop using these devices until receiving updated instructions from the manufacturer.
The AXIOS Stent with Electrocautery-Enhanced Delivery System may have a defective outer sheath that can detach and prevent proper stent expansion, requiring device replacement during the procedure.
Karl Storz uretero-renoscope devices are being recalled because their instructions for reprocessing and sterilization have not been FDA-reviewed or approved. This poses a potential patient safety risk.
Boston Scientific is recalling 1,144 AXIOS Stent Delivery System units because the outer sheath's distal black tip can detach. If this occurs, the tip may remain around the stent saddle and prevent proper stent expansion, requiring device exchange.
Alphatec Spine is recalling Calibrate CCX spinal implants used in fusion procedures after receiving complaints of post-operative implant collapse. Approximately 1,511 implants were distributed nationwide.
Boston Scientific's AXIOS Stent Delivery System is being recalled because the outer sheath can detach during use, preventing proper stent expansion and requiring device exchange.
Medline procedure kits containing surgical masks are recalled nationwide because included masks failed to meet bioburden testing standards, creating potential infection risk during medical procedures.
Karl Storz is recalling 180 ureteroscopes due to instructions for use containing reprocessing procedures that have not been reviewed or approved by the FDA.
The W.S. Badger Company is recalling Badger 50 mineral sunscreen tins lacking the complete drug facts label, barcode, and directions for use. The recall affects 4,834 tins distributed nationwide.
Highland Ridge RV is recalling 2025 Open Range 3X fifth-wheel travel trailers because the vehicle certification label lists the wrong tire size, which could lead to incorrect tire installation.
Temsa is recalling 2024 TS35 vehicles with Cummins L9 engines because fuel filter hoses may separate, causing leaks, engine stalls, and fire or crash risks.
New Flyer is recalling 210 transit buses because fuel filter hoses may separate, causing leaks, engine stalls, and fire risks.
Ford is recalling 2025 Bronco Sport, Escape, and Lincoln Corsair vehicles because the instrument panel may fail to illuminate, increasing crash risk.
Roadtrek is recalling 2023-2025 Westfalia Wave Pop Top vans because incorrect weight labels may lead to unintentional overloading and increased crash risk.
Ford is recalling certain 2021 Expedition, 2021-2022 Super Duty F-250 to F-600 and 2020-2022 Lincoln Corsair vehicles because the rearview camera may display a blank or distorted image.
AMX Global is recalling about 22,500 portable folding stadium seats because security hooks can crack and break, posing fall and injury risks. The company received reports of hook failures including falls and an injury.
Autocar is recalling 2023-2025 E-ACTT vehicles because a software error may cause the vehicle to roll away on an incline or stall the engine.