PlainRecalls
FDA Devices Moderate Class II Terminated

Universal Titanium Prosthesis, Round Head, with Flex H/A titanium shoe. The ear prosthesis is implantable and indicated for hearing loss.

Reported: October 2, 2013 Initiated: August 23, 2013 #Z-2284-2013

Product Description

Universal Titanium Prosthesis, Round Head, with Flex H/A titanium shoe. The ear prosthesis is implantable and indicated for hearing loss.

Reason for Recall

One lot of the product was assembled using the Cam Head version of the same prosthesis instead of the Round head Shaft.

Details

Recalling Firm
Medtronic Xomed, Inc.
Units Affected
60
Distribution
Nationwide Distribution (US), including the states of CA, NE, GA, and IL.
Location
Jacksonville, FL

Frequently Asked Questions

What product was recalled?
Universal Titanium Prosthesis, Round Head, with Flex H/A titanium shoe. The ear prosthesis is implantable and indicated for hearing loss.. Recalled by Medtronic Xomed, Inc.. Units affected: 60.
Why was this product recalled?
One lot of the product was assembled using the Cam Head version of the same prosthesis instead of the Round head Shaft.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 2, 2013. Severity: Moderate. Recall number: Z-2284-2013.