[Recalled] Custom medical procedure packs labeled as: a) STURDI STRAINER TRAY STANDARD, REF '89-5014 — The outer package seal could be open, or compromised which affects the sterilit… | FDA 2023-05-30
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Custom medical procedure packs labeled as: a) STURDI STRAINER TRAY STANDARD, REF '89-5014 |
|---|---|
| Brand / manufacturer | DeRoyal Industries Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2087-2023 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 30 May 2023 |
| EAN / barcode | 50749756217908 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The outer package seal could be open, or compromised which affects the sterility of the procedure pack inside.
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 DeRoyal Industries Inc
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.