Bard¿ Ventralight" ST Mesh with Echo PS TM 7"x9" Reorder Number:… — Class II medical device recall Z-1694-2014
Terminated recall by Davol, Inc., Subs. C. R. Bard, Inc., reported 2014-06-11, distributed nationwide. Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
| Recall number | Z-1694-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Davol, Inc., Subs. C. R. Bard, Inc., Warwick, RI, United States |
| Recall initiated | 2014-04-24 |
| Classified | 2014-06-02 |
| Reported by FDA | 2014-06-11 |
| Terminated | 2015-12-23 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, BE, CA, CH, CY, DE, EE, ES, FI, FR, GB, GR, IE, IT, LU, NL, NO, PL, PT, SE, ZA |
| Reason classes | sterility, packaging |
| Lot numbers | HUXK0899 |
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.
Reason for recall
Pouch holding sterile inflation assembly and inflation adapter may be open or have a weak seal.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1694-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.