Medline sterile surgical kits and trays recalled for potential sterilization issues
Stop using affected Medline surgical kits
Medline Industries has recalled multiple sterile surgical kits and procedure trays due to calibration problems in the sterilization equipment used to manufacture them. Although the products went through normal sterilization cycles, the equipment calibration issues may have reduced the sterility assurance level of these kits. No injuries have been reported.
- Identify any affected Medline convenience kits or surgical trays by checking the model numbers and lot numbers provided by the FDA
- Stop using recalled products immediately
- Contact Medline Industries or your hospital supply chain for instructions on returning or replacing the affected kits
- Check the FDA recall notice for the complete list of 67 affected product models
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-1399-2026More Medline Industries, LP recalls
- FDA-PR2026-08-05Medline Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits recalled for connector overheating risk
- FDA-Device2026-07-29Medline convenience kits with Bard Silastic Foley Catheters recalled for surface contamination
- FDA-Device2026-07-29Medline medical procedure kits recalled for pain medication quality issues
- FDA-Device2026-07-29Medline urology robotic procedure packs recalled for defective Bard Silastic Foley Catheters
- FDA-Device2026-07-29Medline medical convenience kits recalled for potential Bacillus contamination
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