FDA Device recall Z-0687-2020
Elasto-Gel Absorbent Wound Dressing, Item DR8000. 5 Dressings 4" x 4". Sterile
- FDA Device
- Class II
- terminated
- Published 2019-12-25
On 2019-12-25 the FDA classified a Class II recall of Elasto-Gel Absorbent Wound Dressing, Item DR8000. 5 Dressings 4" x 4". Sterile by Southwest Technologies, citing elasto-Gel Wound Dressing may be contaminated with mold.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0687-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-11-18 |
| Published | 2019-12-25 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Southwest Technologies |
| Distribution | CA, GA, IL, KS, NY, OH, TN, TX, VA |
Product
Elasto-Gel Absorbent Wound Dressing, Item DR8000. 5 Dressings 4" x 4". Sterile. UPC 45713-58000 Bacteriostatic
Reason
Elasto-Gel Wound Dressing may be contaminated with mold.
Identifiers
| code_info | Lot 1917802 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0687-2020%22
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