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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
StatusOngoing
ReasonThere is a possible packaging defect impacting the outer Tyvec pouch that protects the sterile product.
ProductMedline UMBILICAL TRAY W/3.5&5FR CATH, REF UVT1250
Quantity174 units
DistributionUS Nationwide distribution in the state of VA.
Initiated2025-05-15
Classified2025-06-20
Recall numberZ-1995-2025
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-1995-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/96959/

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