[Recalled] Helitene Absorbable Collagen Hemostatic Sponge Helitene is indicated in surgical procedures (other than ophthalmological and urological surgery) as an adjunct to hemostasis when control of bleeding by ligature or conventional
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | Helitene Absorbable Collagen Hemostatic Sponge Helitene is indicated in surgical procedures (other than ophthalmological and urological surgery) as an adjunct to hemostasis when control of bleeding by ligature or conventional procedures is ineffective or impractical. |
|---|---|
| Brand / manufacturer | Integra LifeSciences Corporation |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1290-2013 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 28 March 2013 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Due to the process deviation, product lots in question may have been released with higher levels of pyrogens than permitted by the specifications for the products.
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 Integra LifeSciences 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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