BLAST Bandage — Class II medical device recall Z-2538-2018
Terminated recall by Tactical Medical Solutions, Inc., reported 2018-08-01, distributed in AZ, CA, CO, CT, DC, FL, GA, ID…. Blast Bandages (part# BLAST) with Lot# 0617 were not terminally sterilized.
| Recall number | Z-2538-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Tactical Medical Solutions, Inc., Anderson, SC, United States |
| Recall initiated | 2018-04-17 |
| Classified | 2018-07-25 |
| Reported by FDA | 2018-08-01 |
| Terminated | 2020-07-22 |
| Distributed | 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 |
| Countries outside the US | AT, CA, CH, FR, GB, KE, LV, NL, NZ, PL, SG, TR, ZA |
| Quantity | 1,097 units |
| Lot numbers | 0617 |
Product
BLAST Bandage, sterile.
Reason for recall
Blast Bandages (part# BLAST) with Lot# 0617 were not terminally sterilized.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2538-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.