RSDL — Class I medical device recall Z-0773-2023
Terminated recall by Emergent Protective Products USA Inc, reported 2023-01-18. Complaints of leaking packets were received.
| Recall number | Z-0773-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Emergent Protective Products USA Inc, Hattiesburg, MS, United States |
| Recall initiated | 2022-11-24 |
| Classified | 2023-01-10 |
| Reported by FDA | 2023-01-18 |
| Terminated | 2024-10-07 |
| Countries outside the US | CA, CH |
| Quantity | 4,000 units |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 00817129020013 |
| Lot numbers | 23005060, 23005061, 23005062 |
Product
RSDL (Reactive Skin Decontamination Lotion) Kit, NSN 6505-21-912-5229. Used to remove and/or neutralize chemical warfare agents and T-2 Toxin from the skin.
Reason for recall
Complaints of leaking packets were received.
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-0773-2023. 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.