FDA Device recall Z-1575-2022
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow: a) 25 pack, REF H93866025, b) 100 pack, REF H93866100, c) 25 pack, REF H…
- FDA Device
- Class II
- ongoing
- Published 2022-08-31
On 2022-08-31 the FDA classified a Class II recall of Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow: a) 25 pack, REF H93866025, b) 100 pack, REF H93866100, c) 25 pack, REF H… by Baxter Healthcare, citing there is a potential of the packaging not maintaining a sterile barrier for the tip caps.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1575-2022 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-07-22 |
| Published | 2022-08-31 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow: a) 25 pack, REF H93866025, b) 100 pack, REF H93866100, c) 25 pack, REF H938690025
Reason
There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
Identifiers
| code_info | a) REF H93866025, UDI 00085412478845, ALL LOTS; b) REF H93866100, UDI 00085412478852, ALL LOTS; c) REF H938690025, UDI 00085412479941, ALL LOTS |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1575-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.