[Recalled] Amerigel Wound Dressing Maximum Strength CAT# A2001. Wound management. — Not approved labeling claims (antimicrobial and autolytic debridement) | FDA 2014-07-11
A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.
Recall details
| Product | Amerigel Wound Dressing Maximum Strength CAT# A2001. Wound management. |
|---|---|
| Brand / manufacturer | Amerx Health Care Corp. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2638-2014 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 11 July 2014 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Not approved labeling claims (antimicrobial and autolytic debridement)
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 Amerx Health Care Corp.
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.