FDA Device recall Z-1580-2022
Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Pink, 100 pack, REF H938676100
- 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, Pink, 100 pack, REF H938676100 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-1580-2022 |
| 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, Pink, 100 pack, REF H938676100
Reason
There is a potential of the packaging not maintaining a sterile barrier for the tip caps.
Identifiers
| code_info | REF H938676100, UDI 00085412479859, 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-1580-2022%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.