RegWardenFDA facility compliance records
Recall

Class II — Medline Industries, LP

Recalling firmMedline Industries, LP
Registered facilityView this company's 31 registered facilities → (openFDA recall records do not name a specific facility)
ClassificationClass II
StatusOngoing
ReasonDiscrepancy in the shelf-life of a component
ProductMedline convenience kit labeled as: FOOT ANKLE. Medline Kit SKU DYNJ65395A
Quantity30 kits
DistributionUS Nationwide distribution in the state of NY.
Initiated2026-09-11
Classified2026-10-15
Recall numberZ-0189-2027
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-29. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Medline Industries, LP (Z-0189-2027).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-29. https://regwarden.com/recall/99983/

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