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Recall Observatory FDA recall evidence

Device product

NEO-KATH(TM) Caudal Set, REF 201-2430, Sterile

Z-2313-2021

December 28, 2017

Class II

Product summary

Firm
Epimed International
Event
Event 88317
Status
Completed
Classification
Class II
Quantity
140 units
Official record key
device-enforcement:Z-2313-2021

Official wording

Reason: Potential for stylet to protrude from the distal end of the catheter

Code information: Reference Number 201-2430, Lot Numbers 16308139 (Expiration August 2022), 16308383 (Expiration October 2022)

Distribution pattern: Worldwide distribution, with US distribution to CA, DE, OH, OK, PA, VA, WA, WV. International distribution to Canada and Iran.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Potential for stylet to protrude from the distal end of the catheter