FDA Device recall Z-1507-2018
T5 Zipper Toga with Peel-Away Face Shield, (L/XL)
- FDA Device
- Class II
- terminated
- Published 2018-05-02
On 2018-05-02 the FDA classified a Class II recall of T5 Zipper Toga with Peel-Away Face Shield, (L/XL) by Stryker Instruments Div, citing separation of material layers may occur, causing a potential risk of exposure to contaminants.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1507-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-02-23 |
| Published | 2018-05-02 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Stryker Instruments Div |
| Distribution | US |
Product
T5 Zipper Toga with Peel-Away Face Shield, (L/XL); Catalog number: 0400-820-100 Sterile personal protection garment
Reason
Separation of material layers may occur, causing a potential risk of exposure to contaminants.
Identifiers
| code_info | Lot numbers: 17061816, 17061836, 17061839, 17061853, 17071921, 17072017, 17102944, 17102948, 17113081, 17113141, 17113194 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1507-2018%22
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