FDA Device recall Z-2083-2020
NelDerm Hydrogel Dressing (Dressing: 6 x 6
- FDA Device
- Class II
- ongoing
- Published 2020-05-27
On 2020-05-27 the FDA classified a Class II recall of NelDerm Hydrogel Dressing (Dressing: 6 x 6 by Nelson Innovaions, citing foreign material near or along the edge of the hydrogel adhesive within the pouch packaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2083-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2020-02-11 |
| Published | 2020-05-27 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Nelson Innovaions |
| Distribution | CA, NC, PR |
Product
NelDerm Hydrogel Dressing (Dressing: 6 x 6 ; Pad: 4 x 4 ) Product #: HB66T
Reason
Foreign material near or along the edge of the hydrogel adhesive within the pouch packaging
Identifiers
| code_info | Lot #90971 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2083-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.