Summary
The FDA issued a Class II for ARCH Leg Positioning System by Innovative Orthopedic Technologies, LLC. Reason: Due to the holes not being bored to the specific diameter, the locking pins are unable to engage under a load..
Details
Source
Device Recall
External ID
Z-0072-2022
Action Date
2021-10-13
Status
Terminated
Category
device
Product Description
ARCH Leg Positioning System
Lot/Code Info: Model: 6813010 Serial Numbers: 6813010.0066; 6813010.0067; 6813010.0069; 6813010.0070; 6813010.0071; 6813010.0072; 6813010.0073; 6813010.0074; 6813010.0075; 6813010.0076;
Quantity Affected: 10 units
Reason for Recall
Due to the holes not being bored to the specific diameter, the locking pins are unable to engage under a load.
Distribution
U.S. Nationwide distribution in the states of AL, AZ, FL, MI, MN, OK, SD, and TX.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-09-13
Company
Winnie, TX
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 192 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 (Innovative Orthopedic Technologies, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Innovative Orthopedic Technologies, LLC have FDA actions?
This is the only FDA action we have on record for Innovative Orthopedic Technologies, LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-0072-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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