VERITAS Collagen Matrix — Class II medical device recall Z-0807-2021
Terminated recall by Baxter Healthcare Corporation, reported 2021-01-20, distributed nationwide. VERITAS Collagen Matrix 12x25 cm Patches may have undersized width dimensions.
| Recall number | Z-0807-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2020-12-11 |
| Classified | 2021-01-08 |
| Reported by FDA | 2021-01-20 |
| Terminated | 2023-03-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, GB, PL |
| Quantity | 192 units |
| UPC / GTIN / UDI-DI | 00085412531274 |
| Lot numbers | SP19K25-1412935, SP19K25-1412937, SP19L09-1415842, SP20A15-1421512, SP20A16-1421898, SP20B18-1429818, SP20B20-1430375, SP20C27-1439804, SP20C27-1439818, SP20D01-1440793, SP20D28-1447333, SP20E28-1454035, SP20F22-1459746, SP20G08-1462458, SP20G14-1463550, SP20G14-1463552, SP20G14-1463605, SP20G21-1465131, SP20I03-1474281, SP20I08-1474874, SP20I08-1474885, SP20I08-1474895 |
Product
VERITAS Collagen Matrix - Product Usage: intended for use in reconstruction of the pelvic floor excluding transvaginal pelvic organ prolapse and for use in the repair of rectal prolapse excluding rectocele.
Reason for recall
VERITAS Collagen Matrix 12x25 cm Patches may have undersized width dimensions.
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-0807-2021. 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.