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Ovitex® PRS
AROA BIOSURGERY LIMITED · Model R20253-1020G · UDI-DI 09421905067799
10
510(k) clearances
170,422
Adverse events (863 deaths)
73
Recalls
141
Facilities
Description
Ovitex® PRS is for implantation to reinforce soft tissue where weakness exists in patients requiring soft tissue repair or reinforcement in plastic and reconstructive surgery. The device is supplied sterile and is intended for one-time use.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-07-03 | W.L. Gore & Associates, Inc. | Devices were labeled with an expiration date of four years and ten days rather than the validated two years. |
| 2023-04-25 | Davol, Inc. | Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequa |
| 2023-04-25 | Davol, Inc. | Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequa |
| 2023-04-25 | Davol, Inc. | Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequa |
| 2023-04-25 | Davol, Inc. | Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequa |
| 2023-01-11 | Covidien, LP | Collagen film was placed on the opposite side of the mesh may cause delay to treatment/therapy, adhesions, erosion/migration, pain, fistula, hernia (recurrence), and failure of imp |
| 2022-08-12 | Chamberlain Technologies LLC | Potential presence of residual adhesive material on the mesh surface. |
| 2022-08-12 | Chamberlain Technologies LLC | Potential presence of residual adhesive material on the mesh surface. |
| 2022-08-12 | Chamberlain Technologies LLC | Potential presence of residual adhesive material on the mesh surface. |
| 2022-08-12 | Chamberlain Technologies LLC | Potential presence of residual adhesive material on the mesh surface. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.