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U.S. Department of Health and Human Services

Class 2 Device Recall Dorado Straight Impactor

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 Class 2 Device Recall Dorado Straight Impactorsee related information
Date Initiated by FirmMay 10, 2008
Date PostedJune 05, 2013
Recall Status1 Terminated 3 on October 08, 2014
Recall NumberZ-1482-2013
Recall Event ID 64991
Product Classification Impactor - Product Code HWA
ProductStraight Impactor - Dorado IBC, Part Number: SI02140. The device is used to position implants after they have been inserted into the disc space during implantation of intervertebral body fusion devices.
Code Information Lot number: 20856
FEI Number 3005977257
Recalling Firm/
Manufacturer		 SpineFrontier, Inc.
500 Cummings Ctr Ste 3500
Beverly MA 01915-6516
For Additional Information ContactNicole Baginski
978-232-3990
Manufacturer Reason
for Recall		During two separate occasions an impactor plate on the handle broke off while being struck by a mallet.
FDA Determined
Cause 2		Process design
ActionFirm states they notified consignees of recall between 5/10/08 and 5/22/2008. Zero product is currently in distribution.
Quantity in Commerce10
DistributionWorldwide distribution: US (nationwide) to states of: CO, MA, and TX; and country of: Jamaica.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 �7.55.
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