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Recall Observatory FDA recall evidence

Device product

BARDEX I.C. Anti-Infective 2-Way 3cc Foley Catheter, Rx only. Intended for urinary bladder drainage in female patients requiring catheterization for management of incontinence, voiding dysfunction and surgical procedure.

Z-1357-2016

December 18, 2015

Class II

Product summary

Firm
C.R. Bard, Inc.
Event
Event 72922
Status
Terminated
Classification
Class II
Quantity
1,428,000 units (total)
Official record key
device-enforcement:Z-1357-2016

Official wording

Reason: Labeling error: Catalog contains Instructions for Use (IFU) error; incorrect inflation volume.

Code information: Catalog numbers: 0165I108 and 065SI10; All lot numbers produced with IFU (PK7634040) are affected.

Distribution pattern: Distributed US (nationwide) and the countries of Canada and Australia.

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    Labeling error