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Recall Observatory FDA recall evidence

Device product

TRYX Neuro Absorbable Antibacterial Envelope Product Usage: Indicated for stabilization of implanted pacemakers (IPG) and/or implantable cardioverter defibrillators (ICD)

Z-2541-2016

June 29, 2016

Class II

Product summary

Firm
TYRX Inc.
Event
Event 74672
Status
Terminated
Classification
Class II
Quantity
194 units
Official record key
device-enforcement:Z-2541-2016

Official wording

Reason: TRYX products are being recalled since the processes of spaying, welding, drying oven and polymer were not adequately validated.

Code information: model number NMRM6122 lot number 16E03727 16E05728 model number NMRM6133 lot number 16E02726 16E09730

Distribution pattern: US Nationwide Distribution

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    TRYX products are being recalled since the processes of spaying, welding, drying oven and polymer were not adequately validated.