FDAClass IIJune 10, 2020

Vital MIS Spinal Fixation system implants CANN POLY EXT recall

Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 6.5X40MM, Item Number 810M6540 - Product Usage: are non-cervical spinal fixation devices…

Why was Vital MIS Spinal Fixation system implants CANN POLY EXT recalled?

There are reports of inadequate locking of the extended tab screws. Complaints were reported where the closure top backed out of the screw post-operatively.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI: (01)00887868324857; Lot Numbers: C19H0014 C19I0015 C19J0013 C19K0011 C19L0012 C19L0015 C19L0016 SBM108409 SBM118991 SBM122159

Product
Vital MIS Spinal Fixation system implants CANN POLY EXT TAB 6.5X40MM, Item Number 810M6540 - Product Usage: are non-cervical spinal fixation devices…
Recalling firm
Zimmer Biomet, Inc.
Quantity
3235 total
Distribution
US nationwide distribution.
Recall date
June 10, 2020
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls