Recall Z-1395-2024— Emergency Products & Research
Class II · Ongoing
Class II FDA medical device recall by Emergency Products & Research, initiated 2024-02-27. FDA's recall record names no specific 510(k) clearance for this event. Product: O.T.D - Optimum Traction Device - Street Orange. Single use traction splint.. Reason: Failure of adhesive to secure the pole insert..
- Recalling firm
- Emergency Products & Research
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-02-27
- Firm location
- Kent, OH, United States
Product description
O.T.D - Optimum Traction Device - Street Orange. Single use traction splint.
Reason for recall
Failure of adhesive to secure the pole insert.
Data sourced from openFDA. This site is unofficial and independent of the FDA.