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Recall Observatory FDA recall evidence

Device product

FEMORAL ARTERY PACK-LF. Sterile Procedural Tray

Z-1065-2023

November 17, 2022

Class II

Product summary

Firm
MEDLINE INDUSTRIES, LP - Northfield
Event
Event 91386
Status
Ongoing
Classification
Class II
Quantity
15 cases (30 units)
Official record key
device-enforcement:Z-1065-2023

Official wording

Reason: Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.

Code information: Item Number: DYNJ0826625Q, Case UDI/GTIN: 40193489377942, Unit UDI/GTIN: 10193489377941, Lot Number: 22KMA163, 22JME722

Distribution pattern: Worldwide distribution - US Nationwide and the countries of Canada, Japan, Mexico, Panama, Turks & Caicos, United Arab Emirates.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.