FDA Device recall Z-0948-2022
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow, REF H93866100, 100 slip tip caps/package
- FDA Device
- Class II
- terminated
- Published 2022-04-27
On 2022-04-27 the FDA classified a Class II recall of Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow, REF H93866100, 100 slip tip caps/package by Baxter Healthcare, citing product is mislabeled as self-righting Luer slip tip caps, yellow.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0948-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-02-25 |
| Published | 2022-04-27 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow, REF H93866100, 100 slip tip caps/package.
Reason
Product is mislabeled as self-righting Luer slip tip caps, yellow.
Identifiers
| code_info | Lot numbers 60268365, 60268609, 60268610, exp. date 10/31/2023; UDI 0085412478852. |
|---|
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-0948-2022%22
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