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U.S. Department of Health and Human Services

Class 2 Device Recall Vector TAS Modular Driver

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 Class 2 Device Recall Vector TAS Modular Driversee related information
Date Initiated by FirmDecember 12, 2011
Date PostedNovember 05, 2012
Recall Status1 Terminated 3 on November 05, 2012
Recall NumberZ-0205-2013
Recall Event ID 63412
Product Classification Instruments, dental hand - Product Code DZN
ProductVector TAS Modular Driver, a manual driver for Vector TAS dental screws.
Code Information Part Numbers 601-0007 and 601-0010, all lots
FEI Number 2016150
Recalling Firm/
Manufacturer		 Ormco/Sybronendo
1332 S Lone Hill Ave
Glendora CA 91740-5339
For Additional Information Contact
909-962-5600
Manufacturer Reason
for Recall		The Instructions For Use (IFUs) for Vector TAS Modular Driver for some foreign language sections incorrectly lists the sterilization temperature as 130C. The correct sterilization temperature should be listed as 132C and/or 270F.
FDA Determined
Cause 2		Error in labeling
Action"Urgent - Medical Device Correction" letters dated 12/12/2011 were sent via USPS 1st class mail to all customers and again on 2/21/2012 for recall expansion. The device issue was described and recommended actions were provided. Customers were instructed to acknowledge and complete the Return Form. Questions were referred to (800) 854-1741.
Quantity in Commerce4,543
DistributionWorldwide distribution, including Nationwide (USA) and the countries of Canada, Austria, Belgium, Bulgaria, Switzerland, Germany, Denmark, France, Estonia, Spain, Finland, Iceland, United Kingdom, Greece, Croatia, Hungary, Ireland, Italy, Luxembourg, Netherlands, Monaco, Poland, Romania, Serbia, Slovenia, Turkey, Jersey, and Martinique.
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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