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Recall Observatory FDA recall evidence

Device product

HENRY SCHEIN, ILR Insertion Tray, Item No.570-3131

Z-0534-2023

November 02, 2022

Class II

Product summary

Firm
Stradis Medical, LLC dba Stradis Healthcare
Event
Event 91124
Status
Ongoing
Classification
Class II
Quantity
140 units
Official record key
device-enforcement:Z-0534-2023

Official wording

Reason: Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.

Code information: UDI/DI (case) H65857031311, UDI/DI (kit)M75257031310, Serial/Lot Numbers: 22257490596

Distribution pattern: US nationwide distribution, and Canada.

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    bag being incompletely sealed, which may result in a breach
  • Sterility assurance

    reason.sterility_assurance · v1.0.0

    bag being incompletely sealed, which may result in a breach in the sterility