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Recall Observatory FDA recall evidence

Device product

Glow 'N Tell 20 cm Tape: 1100-00 (100 strips); 1100-50 (50 strips); 1100-20 (20 strips). Intended to be placed on the skin to assist during imaging procedures.

Z-1055-2013

March 18, 2013

Class II

Product summary

Firm
LeMaitre Vascular, Inc.
Event
Event 64704
Status
Terminated
Classification
Class II
Quantity
13560
Official record key
device-enforcement:Z-1055-2013

Official wording

Reason: Devices were not sealed correctly during the manufacturing process, and the sterility of these products have been compromised.

Code information: SGL1190, exp 2017-02; SGL1196, exp 2017-09; SGL1197, exp. 2017-09

Distribution pattern: Worldwide Distribution-USA (nationwide) and the countries of Canada, EU, and Asia.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Devices were not sealed correctly during the manufacturing process, and the sterility of these products have been compromised.