Class II — Emergency Products & Research
| Recalling firm | Emergency Products & Research, Inc. |
|---|---|
| Registered facility | Emergency Products & Research, Inc. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Failure of adhesive to secure the pole insert. |
| Product | O.T.D - Optimum Traction Device - Street Orange. Single use traction splint. |
| Quantity | 190,000 units |
| Distribution | US Nationwide distribution in the states of CA, CO, FL, GA, IL, IN, KS, MA, MI, NJ, NY, OH, OK, PA, SC, TX, UT, VA, WA. |
| Initiated | 2024-02-27 |
| Classified | 2024-03-28 |
| Recall number | Z-1395-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Emergency Products & Research (Z-1395-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/94207/
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