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.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1227-2015%22
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