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Recall Observatory FDA recall evidence

Device product

Bard¿ Ventralight" ST Mesh with Echo PS TM 7"x9" Reorder Number: 5955790 Indicated for use in the reconstruction of soft tissue deficiencies, such as the repair of hernias.

Z-1694-2014

April 24, 2014

Class II

Product summary

Firm
Davol, Inc., Subs. C. R. Bard, Inc.
Event
Event 68124
Status
Terminated
Classification
Class II
Quantity
Unavailable
Official record key
device-enforcement:Z-1694-2014

Official wording

Reason: Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.

Code information: Lot Number: HUXK0899

Distribution pattern: Worldwide Distribution - USA (nationwide) and Internationally to AUSTRIA, BELGIUM, CANADA, CYPRUS, ESTONIA, FINLAND, FRANCE, GERMANY, GREECE, IRELAND, ITALY, LUXEMBOURG, NETHERLANDS, NORWAY, POLAND, PORTUGAL, SOUTH AFRICA, SPAIN, SWEDEN, SWITZERLAND, and UNITED KINGDOM

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    weak seal