FDA Device recall Z-1576-2022
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Orange: a) 25 pack, REF H93867025, b) 100 pack, REF H93867100
- 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, Orange: a) 25 pack, REF H93867025, b) 100 pack, REF H93867100 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-1576-2022 |
| 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, Orange: a) 25 pack, REF H93867025, b) 100 pack, REF H93867100
Reason
There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
Identifiers
| code_info | a) REF H93867025, UDI 00085412478869, ALL LOTS; b) REF H93867100, UDI 00085412478890, 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-1576-2022%22
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