FDA Device recall Z-1505-2018
T4 Zipper Toga (S/M)
- FDA Device
- Class II
- terminated
- Published 2018-05-02
On 2018-05-02 the FDA classified a Class II recall of T4 Zipper Toga (S/M) 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-1505-2018 |
| 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
T4 Zipper Toga (S/M); Catalog Number: 0400-810-000 Sterile personal protection garment
Reason
Separation of material layers may occur, causing a potential risk of exposure to contaminants.
Identifiers
| code_info | Lot number: 17061794 |
|---|
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-1505-2018%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.