Medline surgical convenience kits recalled for potential sterilization defect
Check Medline surgical kits for sterilization issue
Medline has recalled multiple surgical convenience kits used in orthopedic and neurosurgery procedures due to calibration issues with sterilization equipment. While the kits went through sterilization cycles, equipment calibration problems may have affected their sterility assurance. No injuries have been reported.
- Check your inventory for Medline convenience kits matching the recalled model numbers and lot numbers
- Do not use recalled kits; quarantine them and contact Medline or your supplier for instructions
- Review the FDA recall notice for the complete list of affected model numbers and lot numbers
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1421-2026More Medline Industries, LP recalls
- FDA-Device2026-06-03Medline EYE TRAY-LF medical kit recalled for mismatched syringes
- FDA-Device2026-06-03Medline spinal anesthesia and nerve block kits recalled for bupivacaine quality and efficacy concerns
- FDA-Device2026-05-20Medline Namic Preceptor blood pressure manifold recalled for particulate contamination
- FDA-Device2026-05-20Medline TAVI medical convenience kits recalled for particulate contamination in fluid path
- FDA-Device2026-05-20Medline medical convenience kits with Namic Manifold recalled for particulate contamination
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