Data Foundry

Medical device recalls 2013

Multi Vector Distractor Pin Holding Clamp — Class II medical device recall Z-1745-2013

Terminated recall by Synthes USA HQ, Inc., reported 2013-07-24, distributed nationwide. Synthes is initiating a voluntary Medical Device removal for specified part numbers and lot numbers of the Mut

Recall numberZ-1745-2013
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmSynthes USA HQ, Inc., West Chester, PA, United States
Recall initiated2013-05-31
Classified2013-07-17
Reported by FDA2013-07-24
Terminated2015-08-31
DistributedNationwide (US)
Quantity121
Lot numbers3769706, 3769720, 3779569, 3779571, 3788731, 3788741, 3794434, 7806093, 7806096, 7823463, 7823464
Model numbers487.941, 487.942

Product

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.

Reason for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1745-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.