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
ReasonComponent labeling discrepancy
ProductMedline medical convenience kit labeled as: TRACH TUBE KIT, Medline Kit SKU DYKM2330
Quantity45 kits
DistributionUS Nationwide distribution in the state of California.
Initiated2026-07-10
Classified2026-08-21
Recall numberZ-2999-2026
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Medline Industries, LP (Z-2999-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99506/

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