RegWardenFDA facility compliance records
Recall

Class II — MEDLINE INDUSTRIES, LP - Northfield

Recalling firmMedline Industries, LP
Registered facilityView this company's 31 registered facilities → (openFDA recall records do not name a specific facility)
ClassificationClass II
StatusTerminated
ReasonProduct stored incorrectly in temperature controlled setting instead of refrigeration.
ProductHARDY DIAGNOSTICS CatScreen, 25dsk/vial
Quantity100 units (4 packs, 25 per pack)
DistributionUS Nationwide distribution in the state of California.
Initiated2021-12-01
Classified2022-02-02
Terminated2023-01-09
Recall numberZ-0554-2022
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 - Northfield (Z-0554-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/89151/

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