FDA Device recall Z-0941-2020
Safeline Y-Type Blood Set, Catalog Number V2500
- FDA Device
- Class II
- terminated
- Published 2020-02-12
On 2020-02-12 the FDA classified a Class II recall of Safeline Y-Type Blood Set, Catalog Number V2500 by B Braun Medical, citing potential for leakage at the joint between the blood filters and tubing.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0941-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-11-20 |
| Published | 2020-02-12 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | B Braun Medical |
| Distribution | US |
Product
Safeline Y-Type Blood Set, Catalog Number V2500
Reason
Potential for leakage at the joint between the blood filters and tubing
Identifiers
| code_info | GUIDID: 04046964188633 Lot Numbers: 61674884 - Expiration Date: April 30, 2024, 61677634 - Expiration Date: April 30…GUIDID: 04046964188633 Lot Numbers: 61674884 - Expiration Date: April 30, 2024, 61677634 - Expiration Date: April 30, 2024, 61678262 - Expiration Date: May 31, 2024, 61680625 - Expiration Date: May 31, 2024, 61685110 - Expiration Date: June 30, 2024 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0941-2020%22
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