EASYGRIP FLO-41 US — Class II medical device recall Z-2051-2021
Terminated recall by Baxter Healthcare Corporation, reported 2021-07-21. There is a discrepancy in the expiry date encoded into the 2D barcode. The correct expiration date is the huma
| Recall number | Z-2051-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2021-06-15 |
| Classified | 2021-07-09 |
| Reported by FDA | 2021-07-21 |
| Terminated | 2024-01-12 |
| Countries outside the US | AU, BE, CY, ES, GB, HK, IE, IT, NL, NO, NZ, PT, SE |
| Quantity | 4,752 units |
| Lot numbers | 0000266641, 0000325839, 0000362640, 0000380266 |
Product
EASYGRIP FLO-41 US. For delivering hemostatic agents to bleeding sites through a trocar.
Reason for recall
There is a discrepancy in the expiry date encoded into the 2D barcode. The correct expiration date is the human-readable date
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-2051-2021. 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.