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Class IIOngoing

Medline Industries, LP recalls Medline convenience kit labeled as: FOOT ANKLE

Recall date · record updated Oct 21, 2026 · Source: U.S. Food and Drug Administration (openFDA device enforcement)

What to do

Check your product against the names and codes above. The FDA enforcement record lists the recall as voluntary: firm initiated; it does not state a consumer remedy, so follow the firm’s notice or the FDA link.

Company
Medline Industries, LP
Reason
Discrepancy in the shelf-life of a component
Hazard
FDA Class II: may cause temporary or medically reversible adverse health consequences (FDA definition).
Who’s affected
US Nationwide distribution in the state of NY.
Where
Nationwide
Official notice
www.accessdata.fda.gov/scripts/ires/index.cfm?Event=99983…

Products

  1. Medline convenience kit labeled as: FOOT ANKLE. Medline Kit SKU DYNJ65395A

    Codes/lots: UDI/DI 10195327174156 (each) 40195327174157 (case), Lot Number 22GBW912Quantity: 30 kitsRecall no. Z-0189-2027Class II

Update history

  1. First listed on OVERLOOKED from the official record.

When the agency expands or changes this recall, we update this page and log the change here.

Proof: raw official record (JSON) · fetched from FDA API

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