FDA Device recall Z-2641-2014
Amerigel Daily Dressing Advanced 3-in-1 Hydrogel
- FDA Device
- Class II
- terminated
- Published 2014-09-24
On 2014-09-24 the FDA classified a Class II recall of Amerigel Daily Dressing Advanced 3-in-1 Hydrogel by Amerx Health Care, citing not approved labeling claims (antimicrobial and autolytic debridement).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2641-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-07-11 |
| Published | 2014-09-24 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Amerx Health Care |
| Distribution | US |
Product
Amerigel Daily Dressing Advanced 3-in-1 Hydrogel; 30 single used foil packets 1g. each; CAT # A2003. Wound management.
Reason
Not approved labeling claims (antimicrobial and autolytic debridement)
Identifiers
| code_info | Lot codes: 2WD07. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2641-2014%22
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