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Recall Observatory FDA recall evidence

Device product

Pilling Modular Verres Body/Obturator, Product Code 140880

Z-1178-2016

January 08, 2015

Class II

Product summary

Firm
Teleflex Medical
Event
Event 73267
Status
Terminated
Classification
Class II
Quantity
8
Official record key
device-enforcement:Z-1178-2016

Official wording

Reason: Packaging error in which customers who ordered product code 140880 (Verres cannula for use with a separately available needle tip) were incorrectly provided with product code 140878 (Verres cannula with integral needle tip).

Code information: Lot K3

Distribution pattern: US Distribution to the state of : UT

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    Packaging error