FDA Device recall Z-2051-2021
EASYGRIP FLO-41 US. For delivering hemostatic agents to bleeding sites through a trocar
- FDA Device
- Class II
- terminated
- Published 2021-07-21
On 2021-07-21 the FDA classified a Class II recall of EASYGRIP FLO-41 US. For delivering hemostatic agents to bleeding sites through a trocar by Baxter Healthcare, citing there is a discrepancy in the expiry date encoded into the 2D barcode. The correct expiration date is the human-readable date.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2051-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-06-15 |
| Published | 2021-07-21 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Baxter Healthcare |
| Distribution | n/a |
Product
EASYGRIP FLO-41 US. For delivering hemostatic agents to bleeding sites through a trocar.
Reason
There is a discrepancy in the expiry date encoded into the 2D barcode. The correct expiration date is the human-readable date
Identifiers
| code_info | Product Code: ADS201897. Lot Numbers: 0000266641, 0000325839, 0000362640, 0000380266. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2051-2021%22
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