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Recall Observatory FDA recall evidence

Device product

Prep-Fill Guarded Luer Connector (GLC): a. Part Number 57-400, Female Lock - Female Lock Guarded Luer Connector, Sterile; b. Part number 57-400W, Female Lock - Female Lock Guarded Luer Connector, Sterile; c. Part number 57-401, Female Lock - Male Lock Guarded Luer Connector, Sterile; d. Part number 57-402, Female Slip - Female Lock Guarded Luer Connector, Sterile; and e. Part number 57-403, Female Slip - Female Slip Guarded Luer Connector.

Z-0925-2023

September 16, 2022

Class II

Product summary

Firm
International Medical Industries, Inc.
Event
Event 91276
Status
Ongoing
Classification
Class II
Quantity
228,000 DEVICES
Official record key
device-enforcement:Z-0925-2023

Official wording

Reason: Blister package had an unsealed edge compromising sterility.

Code information: a. Part 57-400 - Lot numbers 45266, 44549, 44120, 43800, 43626, 42634, 42236, 39350, 37176, 36596, 33074. UDI: B212574001. b. Part 57-400W - Lot numbers 39371, 37093, 37086, 37079, 39378, 39364, 39357, 36558. UDI: B21257400W1. c. Part 57-401 - Lot numbers 45047, 43633. UDI: B212574011. d. Part 57-402 - Lot number 37151. UDI: B212574021.

Distribution pattern: US Nationwide Distribution was made to AR, AZ, CA, CO, FL, GA, ID, IL, IN, IA, KS, KY, MD, MA, MI, MS, MO, MT, NE, NJ, NY, NC, OH, PA, SC, TX, and VA. There was no government/military/foreign distribution.

Derived failure modes

  • Sterility assurance

    reason.sterility_assurance · v1.0.0

    package had an unsealed edge compromising sterility