FDA-Device2026-10-21Class IIPACKAGING DEFECT
Medline foot-ankle convenience kit recalled for shelf-life component discrepancy
What this means
Medline Industries recalled a foot-ankle convenience kit (SKU DYNJ65395A) because one component in the kit has an incorrect or discrepant shelf-life label. The issue affects 30 kits distributed in New York. No injuries have been reported.
- Check if you have Medline foot-ankle kit SKU DYNJ65395A, Lot 22GBW912.
- Do not use the kit if you have it.
- Contact Medline Industries or your healthcare provider for instructions on return or replacement.
The agency's original wording
Hazard
Discrepancy in the shelf-life of a component
Intended for
All ages
Illnesses reported
None reported
Sold states
US Nationwide distribution in the state of NY.
Affected count
30 kits
Manufactured in
3 Lakes Dr, Northfield, IL, United States
Products
Medline convenience kit labeled as: FOOT ANKLE. Medline Kit SKU DYNJ65395A
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0189-2027More Medline recalls
- FDA-Device2026-10-22Medline medical convenience kits recalled for difficult removal and adhesive residue
- FDA-Device2026-10-22Medline sterile C-section surgical drape recalled for difficult removal and skin adhesive residue
- FDA-Device2026-10-22Medline medical convenience kits recalled for difficult removal and adhesive residue
- FDA-Device2026-10-22Medline surgical convenience kits recalled for difficult removal and adhesive residue
- FDA-Device2026-10-22Medline tubal ligation surgical kit recalled for difficult removal and skin adhesive residue
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