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U.S. Department of Health and Human Services

Class 2 Device Recall Vertier Surgical Table

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 Class 2 Recall
Vertier Surgical Table
see related information
Date Posted April 06, 2010
Recall Status1 Terminated on August 11, 2010
Recall Number Z-1238-2010
Recall Event ID 53993
Product Classification Table, Operating-Room, Ac-Powered - Product Code FQO
Product Vertier Surgical Table, Catalog numbers 0788100000, 0788100000S, 0788100001, and 0788100001S
Code Information All Lots Are Affected
Recalling Firm/
Stryker Communications Corp
1410 Lakeside Pkwy Ste 100
Flower Mound, Texas 75028-4026
Consumer Instructions Contact the recalling firm for information Contact the recalling firm for information
Manufacturer Reason
for Recall
In certain positions, product is susceptible to fluid instrusion which could possibly result in short circuit or unsolicited movement.
FDA Determined
Cause 2
Action Firm notified all consignees by letter sent 11/13/2009. Contact the firm at 972-410-7100 with questions relating to this recall.
Quantity in Commerce 206
Distribution United States (GA, AR, ND, KY, CO, CA, SD, PA, OH, TX, SC, NY, MS, IL, KS, NJ, OR, WA, MN, VA, IL, OK, WY, IN, ID, UT, MO, FL, and DC) and Canada.
Total Product Life Cycle TPLC Device Report

1 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.