Medline surgical convenience kits recalled for sterilization equipment calibration issues
Check Medline surgical kit lot numbers
Medline Industries recalled multiple surgical convenience kits used in hospitals and surgical centers because equipment used to sterilize and package them had calibration problems. Although the kits went through sterilization cycles, the calibration issues may have affected their sterility. No injuries have been reported.
- If you use these kits in a healthcare facility, check your inventory against the affected lot numbers listed in the recall notice
- Contact Medline Industries or your supplier for instructions on returning or replacing affected kits
- Do not use kits from the recalled lot numbers until you receive further guidance
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-1419-2026More 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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