State
73,570 recalls have nationwide distribution and so reach Michigan. 9,551 additional recalls listed Michigan specifically in their distribution scope.
Of the 9,551 recalls naming Michigan we have scored against our rubric, 1,566 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,550 (27%) are Severe.
Which agencies issued them
These figures cover only the 9,551 recalls whose distribution notice names Michigan specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Jenavalve Technology Inc. is recalling 108 units of the JenaValve Trilogy Delivery Catheter due to a defect that may prevent heart valve deployment.
Medtronic is recalling specific Grafton DBM and Grafton Plus DBM products because the donor tissue tested positive for Clostridium butyricum, posing a potential infection risk.
Beckman Coulter is recalling IQ200 SPRINT, SELECT, and ELITE hematology analyzers because a check valve defect may cause fluid leaks, creating slip, chemical, and biohazard risks.
Medline is recalling 193,374 surgical convenience kits nationwide because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.
Medline Industries is recalling 1,900 surgical convenience kits because cannula components do not meet ISO 80369-7 standards and may leak or break during use.
Baxter Healthcare is recalling Likorall Overhead Lifts because a motor shaft breakage combined with reduced safety system performance may cause the lift strap to lower quickly, posing a risk of patient injury.
Becton Dickinson is recalling 553,625 BD Phoenix Panel NMIC-312 units nationwide because the CPO Ambler classification feature may misclassify Klebsiella pneumoniae.
Autocar is recalling 2022-2027 Xpeditor trucks with Cummins L9 engines because fuel hoses may separate, causing leaks, engine stalls, and fire risks.
Medline Industries is recalling 8,374 surgical convenience kits nationwide because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.
Medline is recalling 6,069 surgical convenience kits because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.
Daimler Trucks North America is recalling 2027 Thomas Built Buses Saf-T-Liner C2 school buses because a heater hose may rupture, causing hot coolant to leak and burn occupants.
Sarnova HC is recalling 2,500 Curaplex Capnography kits because they were assembled with pediatric nasal cannulas instead of adult ones.
Medline is recalling 472 surgical convenience kits because the cannula components do not meet ISO 80369-7 requirements, which may cause leaking or breaking during use.
Medline is recalling 3,551 convenience kits containing CONMED AirSeal Access Ports because they may trigger erroneous overpressure alerts and system venting, potentially delaying or ending surgical procedures.
Ferno-Washington is recalling 319 Power F2 Powered Fastening Systems due to a firmware issue that may cause intermittent loss of powered functionality, potentially delaying patient transport.
Medline is recalling 3,551 convenience kits containing CONMED AirSeal Access Ports due to potential for erroneous overpressure alerts and system venting during use.
Teva Pharmaceuticals is recalling Metoclopramide tablets because they may contain foreign tablets or capsules. The affected products were distributed nationwide.
Medline Industries is recalling 1,834 cardiac surgery kits because cannula components do not meet ISO 80369-7 dimensional requirements, which may contribute to leaking or breaking during use.
Medline Industries is recalling 3,551 convenience kits containing CONMED AirSeal Access Ports due to potential overpressure alerts and system venting that may delay or end procedures.
Steris is recalling RAPICIDE PA Part A High-Level Disinfectant because a blocked vented cap may cause the bottle to swell and release vapor or liquid, potentially injuring users.
Intelerad Medical Systems is recalling IntelePACS software versions because reported and displayed images may not match due to a web-browser issue.
American Health Packaging is recalling 5,363 cartons of Metoclopramide Tablets, USP, 5 mg, due to the presence of foreign tablets or capsules.
Medline Industries is recalling 3,551 convenience kits containing CONMED AirSeal Access Ports due to potential erroneous overpressure alerts and system venting.
Medline is recalling 3,125 surgical convenience kits because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.
W L Gore & Associates is recalling 32 units of GORE VIABIL Short Wire Biliary Endoprosthesis because they may be mislabeled with the incorrect length.