FDA Device recall Z-1227-2015
Baxter, Self-Righting Syringe Tip Caps, Self-Righting DISCPAC Syringe Tip Caps
- FDA Device
- Class II
- terminated
- Published 2015-03-11
On 2015-03-11 the FDA classified a Class II recall of Baxter, Self-Righting Syringe Tip Caps, Self-Righting DISCPAC Syringe Tip Caps by Baxter Englewood, citing self-Righting Luer Tip Caps were manufactured and shipped with a missing latex symbol on both single and case labels.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1227-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-12-29 |
| Published | 2015-03-11 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Baxter Englewood |
| Distribution | US |
Product
Baxter, Self-Righting Syringe Tip Caps, Self-Righting DISCPAC Syringe Tip Caps. Product codes H93866100, H93869100, H93866025, H93867025, H93867100, H938671025, H938671100, H938673025, H938673100, H938674025, H938674100, H938676025, H938676100, H938677025, H938677100, H938679025, H938679100, H938690025, H93869025, H938693025, H938696025, H93868025, H93868100, H938672025, H938672100, H938675025, H938675100, H938678025, and H938678100.
Reason
Self-Righting Luer Tip Caps were manufactured and shipped with a missing latex symbol on both single and case labels.
Identifiers
| code_info | All DiscPac products are affected within expiry up to October 2017 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
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FDA Device · Class II · 2016-02-10 · Baxter Englewood - ABACUS SE (Single-Workstation Edition) and ABACUS ME (Multi-Workstation Edition) Product Usage: The ABACUS Software is a Windows-based orde…
FDA Device · Class II · 2015-05-27 · Baxter Englewood - Self-Righting Luer Lock Tip Cap, Green and Self-Righting Luer Slip Tip Cap, Yellow, Baxter Healthcare Corporation, 14445 Grasslands Dr. Eng…
FDA Device · Class II · 2014-12-31 · Baxter Englewood - Abacus 3.1, Pharmacy Calculator Product Usage: Provide pharmacy calculations for automated compounding
FDA Device · Class II · 2014-07-02 · Baxter Englewood
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1227-2015%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.