[Recalled] Disposable Spetzler-Malis Bipolar forceps, 23CM SLM DISP BAYONET 0.5MM, Catalog Number 6780-230-005 — An error was identified on the expiration date of the product label | FDA 2023-09-11
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Disposable Spetzler-Malis Bipolar forceps, 23CM SLM DISP BAYONET 0.5MM, Catalog Number 6780-230-005 |
|---|---|
| Brand / manufacturer | Stryker Corporation |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0255-2024 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 11 September 2023 |
| EAN / barcode | 7613327300307 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: An error was identified on the expiration date of the product label. The shelf life for the products impacted is 36 months (3 years) however the product label represents a 54 month (4.5 year) shelf life.
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 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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