Composix L/P with Echo PS 10" X 13" Product Code 0144113 The Composix… — Class II medical device recall Z-0819-2014
Terminated recall by Davol, Inc., Subs. C. R. Bard, Inc., reported 2014-01-29, distributed nationwide. Product labeling does not match product configuration.
| Recall number | Z-0819-2014 |
|---|---|
| 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 | 2014-01-03 |
| Classified | 2014-01-23 |
| Reported by FDA | 2014-01-29 |
| Terminated | 2015-12-23 |
| Distributed | Nationwide (US) |
| Quantity | 19 |
| Reason classes | labeling |
| Lot numbers | HUXH0294 |
Product
Composix L/P with Echo PS 10" X 13" Product Code 0144113 The Composix L/P Mesh with Echo PS Positioning System is a non-absorbable sterile lightweight mesh prosthesis, with a preattached removable positioning system. This system is indicated and designed for the reconstruction of soft tissue deficiencies during laproscopic ventral hernia repair.
Reason for recall
Product labeling does not match product configuration.
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-0819-2014. 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.