FDA recall record

Synthes USA HQ Multi Vector Distractor Pin Holding Clamp, limited bone stock The holding recall — FDA Z-1745-2013

Synthes is initiating a voluntary Medical Device removal for specified part numbers and lot numbers of the Mutis Vector Distractor Pin Holding clamp,…

Class IIclassification
Z-1745-2013official record ID
Jul 24, 2013report date

Recall record at a glance

Official recordZ-1745-2013
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSynthes USA HQ, Inc.
Report dateJul 24, 2013
Recall initiation dateMay 31, 2013
Quantity121
LocationWest Chester, PA, United States

Official product description

Multi Vector Distractor Pin Holding Clamp, limited bone stock The holding clamp is part of the Multi Vector Distractor which cis used for mandibular bone lengthening, including conditions such as congenital mandibular deficiencies or post-traumatic defects. The Multi Vector Distractor can be utilized to perform bone transport procedures as an alternative to bone grafts and free flaps.

Why the product was recalled

Synthes is initiating a voluntary Medical Device removal for specified part numbers and lot numbers of the Mutis Vector Distractor Pin Holding clamp, limited bone stock. The firm received complaints that the clamp and nut construct would not engage the distractor arm threads and subsequently bind. It is not likely that a serious adverse event will result due to a nonconforming clamp, however there

Distribution information

US Nationwide Distribution including the states of MA, TX, MN, SC, UT, VA, and NY.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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