Medline surgical convenience kits recalled over sterilization equipment calibration issues
Stop using affected Medline surgical kits
Medline has recalled multiple surgical convenience kits used in gynecological, urological, and other surgical procedures due to calibration problems with sterilization equipment. Although the kits went through sterilization cycles, the equipment calibration issues may have affected their sterility assurance level, potentially compromising the sterility of the devices.
- Identify any Medline surgical convenience kits in your facility using the model numbers listed in the full recall notice
- Stop using the affected kits immediately
- Contact Medline Industries for instructions on returning or disposing of the recalled products
- Review your inventory against the complete list of 77 affected model numbers and lot numbers provided by the FDA
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-1415-2026More 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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