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Recall Observatory FDA recall evidence

Device product

BruxZir Shaded, Model No. 70-1167-NOW0001, 70-1167-NOW0002, 70-1167-NOW0003, 70-1167-NOW0005, 70-1167-NOW0006 The device is indicated for use by dental technicians in the construction of custom made all ceramic restorations for anterior and posterior location.

Z-2897-2016

August 15, 2016

Class II

Product summary

Firm
Prismatik Dentalcraft, Inc
Event
Event 75082
Status
Terminated
Classification
Class II
Quantity
150 units
Official record key
device-enforcement:Z-2897-2016

Official wording

Reason: Prismatik Dentalcraft is recalling BruxZir Shaded because the new design was manufactured at risk and were to be quarantined and held until the validation was completed. Prismatik failed to properly identify the lots as quarantined product.

Code information: BZ0004415 BZ0004745 BZ0004416 BZ0004747 BZ0004522 BZ0004360 BZ0004496 BZ0004593 BZ0004094 BZ0004614

Distribution pattern: Nationwide distribution to SC, MN, NC, IN, AZ, OR, WA, CA, WY

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Prismatik Dentalcraft is recalling BruxZir Shaded because the new design was manufactured at risk and were to be quarantined and held until the validation was completed. Prismatik failed to properly identify the lots as quarantined product.