Esmark Elastic Bandage — Class II medical device recall Z-1649-2014
Terminated recall by Medline Industries Inc, reported 2014-05-28, distributed nationwide. This lot did not go through the correct sterilization procedures. This product may potentially be non-sterile.
| Recall number | Z-1649-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries Inc, Mundelein, IL, United States |
| Recall initiated | 2014-03-20 |
| Classified | 2014-05-21 |
| Reported by FDA | 2014-05-28 |
| Terminated | 2017-11-29 |
| Distributed | Nationwide (US) |
| Quantity | 2,860 bandages |
| Reason classes | sterility |
| Lot numbers | 13LA1009 |
| Model numbers | DYNJ05116A |
Product
Esmark Elastic Bandage (Sterile), 4" x 9'. Item DYNJ05116A, Individually wrapped, 20 bandages per case. Packaged by Medline Industries Inc. This product is used as an elastic bandage to support and compress a part of a patient's body. It is also used as a tourniquet to restrict blood flow to a part of a patient's body.
Reason for recall
This lot did not go through the correct sterilization procedures. This product may potentially be non-sterile.
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-1649-2014. 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.