Medline surgical gowns recalled for sterilization equipment calibration issues
What this means
Medline has recalled multiple models of surgical gowns due to calibration problems with sterilization equipment. While the gowns went through sterilization cycles, equipment calibration issues may have affected their sterility. No injuries have been reported.
- Check if you have any Medline surgical gowns with model numbers DYNJP2001 through DYNJP2503 or similar variants
- Stop using affected gowns immediately
- Contact Medline or your supplier for instructions on return or replacement
- Refer to the FDA notice for the complete list of affected lot numbers and model numbers
The agency's original wording
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-1424-2026More Medline recalls
- FDA-Device2026-09-09Medline Convenience Kits recalled for potential sterility breach in antiseptic applicators
- FDA-Device2026-09-09Medline Convenience Kits with BD ChloraPrep Clear applicators recalled for contamination risk
- FDA-Device2026-09-09Medline Convenience Kits recalled for sterility packaging breach risk
- FDA-Device2026-09-09Medline Convenience Kits with BD ChloraPrep Clear applicators recalled for defective packaging seals
- FDA-Device2026-09-09Medline Arterial Line Insertion Kit recalled for sterility packaging breach risk
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