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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:152778

12 mm Distraction Pin, Blunt Qty: 1 per pack; STERILE; Manufactured for: Medline Industries, Inc., Mundelein, IL 60060 USA Distraction Pin is designed for Anterior Cervical Fusion Procedures. Use with vertebral body distraction instruments. It is intended as a temporary fixation screw utilized during cervical spine procedures.

Official recall number

Z-2107-2017

Evidence summary

Product code
LXH
Recall status
Terminated
Event initiated
December 14, 2016
Root cause
Process control
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-2107-2017

Field note

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