O.T.D - Optimum Traction Device - Street Orange. Single use traction splint.
Summary
The FDA issued a Class II for O.T.D - Optimum Traction Device - Street Orange. Single use traction splint. by Emergency Products & Research. Reason: Failure of adhesive to secure the pole insert..
Details
Source
Device Recall
External ID
Z-1395-2024
Action Date
2024-04-03
Status
Ongoing
Category
device
Product Description
O.T.D - Optimum Traction Device - Street Orange. Single use traction splint.
Lot/Code Info: Model EP-800; Lot No. 20230523-04, 09082023-11, 09082023-12, 122023-3, 122023-2, 122023-1.
Quantity Affected: 190,000 units
Reason for Recall
Failure of adhesive to secure the pole insert.
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-02-27
Company
Kent, OH
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 163 device recalls issued in the same week, part of 403 device-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Emergency Products & Research) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Emergency Products & Research have FDA actions?
This is the only FDA action we have on record for Emergency Products & Research in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1395-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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