Bard¿ PerFix Light Plug The Bard¿ PerFix Light Plug is indicated for… — Class II medical device recall Z-0191-2015
Terminated recall by Davol, Inc., Subs. C. R. Bard, Inc., reported 2014-11-19, distributed in CA, DE, MD, MN, MO, NM, OH, UT. The patient record peel-off label product code and size did not match the other labeling and actual product in
| Recall number | Z-0191-2015 |
|---|---|
| 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 | 2014-10-08 |
| Classified | 2014-11-07 |
| Reported by FDA | 2014-11-19 |
| Terminated | 2015-12-23 |
| Distributed | CA, DE, MD, MN, MO, NM, OH, UT |
| Quantity | 78 units |
| Reason classes | labeling |
| Lot numbers | HUYD0176 |
Product
Bard¿ PerFix Light Plug The Bard¿ PerFix Light Plug is indicated for reinforcement if soft tissue, where weakness exists, in procedures involving soft tissue repair, such as groin hernia defects.
Reason for recall
The patient record peel-off label product code and size did not match the other labeling and actual product in the packaging for the Bard Small PerFix Light Plug.
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-0191-2015. 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.