[Recalled] T4 Zipper Toga (S/M); Catalog Number: 0400-810-000 Sterile personal protection garment — Separation of material layers may occur, causing a potential risk of exposure t… | FDA 2018-02-23
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | T4 Zipper Toga (S/M); Catalog Number: 0400-810-000 Sterile personal protection garment |
|---|---|
| Brand / manufacturer | Stryker Instruments Div. of Stryker Corporation |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1505-2018 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 23 February 2018 |
| EAN / barcode | 17061794 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Separation of material layers may occur, causing a potential risk of exposure to contaminants.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Stryker Instruments Div. of Stryker Corporation
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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