FDA Device recall Z-2538-2018
BLAST Bandage, sterile
- FDA Device
- Class II
- terminated
- Published 2018-08-01
On 2018-08-01 the FDA classified a Class II recall of BLAST Bandage, sterile by Tactical Medical Solutions, citing blast Bandages (part# BLAST) with Lot# 0617 were not terminally sterilized.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2538-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-04-17 |
| Published | 2018-08-01 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Tactical Medical Solutions |
| Distribution | AL, AZ, CA, CO, CT, DC, FL, GA, ID, IL, IN, KS, KY, MA, MD, ME, MI, MO, MS, NC, ND, NM, NY, OH, PA, SC, TX, VA, WI |
Product
BLAST Bandage, sterile.
Reason
Blast Bandages (part# BLAST) with Lot# 0617 were not terminally sterilized.
Identifiers
| code_info | Lot 0617 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2538-2018%22
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