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U.S. Department of Health and Human Services

Class 2 Device Recall Stryker MIS Bur, 2.0mm Neuro Diamond

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  Class 2 Device Recall Stryker MIS Bur, 2.0mm Neuro Diamond see related information
Date Initiated by Firm July 06, 2009
Date Posted January 11, 2010
Recall Status1 Terminated 3 on October 25, 2010
Recall Number Z-0595-2010
Recall Event ID 53982
510(K)Number K032303  K040300  
Product Classification Drills, burrs, trephines & accessories (simple, powered) - Product Code HBE
Product Stryker MIS Bur, 2.0mm Neuro Diamond, sterile, Stryker Instruments, Kalamazoo, MI; REF 8420-107-120.
Code Information All lots distributed 1/30/06 through 3/4/09. Lots 06004017, 06034017, 06075017, 06086017, 06206017, 07002017, 07039017, 07067017, 07121017, 07219017, 07279017, 07320017, 07346017, 08007017, 08030017, 08044017, 08081017, 08205017, 08275017 and 09043017.
Recalling Firm/
Stryker Instruments Div. of Stryker Corporation
4100 E. Milham Ave.
Kalamazoo MI 49001
For Additional Information Contact
800-800-4236 Ext. 3808
Manufacturer Reason
for Recall
The bur may fracture, resulting in fragments within the surgical site, injury to the patient or surgical team, or both.
FDA Determined
Cause 2
Device Design
Action Consignees were sent a letter dated 7/10/09 instructing them to locate and return product on hand for replacement. Surgeons who use the product were notified via a separate, untitled letter, dated July 13, 2009. A speed warning will be added to the product labels. Questions are directed to the firm at: 1-800-800-4236 ext. 3808.
Quantity in Commerce 5438 of all products
Distribution Nationwide distribution: Australia, Canada, England, France, Hong Kong, Japan, Netherlands, South Africa, Sweden, Switzerland and Taiwan.
Total Product Life Cycle TPLC 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.
510(K) Database 510(K)s with Product Code = HBE and Original Applicant = STRYKER INSTRUMENTS