[Recalled] Hartmann Econolux Ref 416 105 Sterile Gauze sponge 4"x4" 12-ply 24 boxes/case 1200 total sponges For use in wound cleansing, debriding of wounds, wound packing, covering and swabbing — Micro holes were detected in the lam
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Hartmann Econolux Ref 416 105 Sterile Gauze sponge 4"x4" 12-ply 24 boxes/case 1200 total sponges For use in wound cleansing, debriding of wounds, wound packing, covering and swabbing |
|---|---|
| Brand / manufacturer | Hartmann USA, Inc |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1857-2012 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 14 May 2012 |
| EAN / barcode | 101546391 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Micro holes were detected in the laminate of the sterile barrier system of sterilized Hartmann Econolux and Hartmann Sterilux gauze 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 →
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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