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U.S. Department of Health and Human Services

Class 2 Device Recall SwitchPoint Element (SPE) Control System

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 Class 2 Device Recall SwitchPoint Element (SPE) Control Systemsee related information
Date Initiated by FirmApril 15, 2010
Date PostedMay 21, 2010
Recall Status1 Terminated 3 on January 24, 2011
Recall NumberZ-1643-2010
Recall Event ID 55477
510(K)NumberK031068 K033132 
Product Classification General & Plastic Surgery Laparoscope - Product Code GCJ
ProductSwitchPoint Element (SPE) Control System. Control System for audio/video, surgical, and room equipment. Catalog Numbers: 067000220, 067000230, 067000231, 067000232, 067000233. Used for direct control of room equipment, audio/video equipment, and indirect control of surgical equipment in the operating room.
Code Information Product installed Between January 1, 2008 and August 31, 2009.
Recalling Firm/
Manufacturer		 Stryker Communications Corp
1410 Lakeside Pkwy Ste 100
Flower Mound TX 75028-4026
For Additional Information Contact
972-410-7310
Manufacturer Reason
for Recall		Installation records are incomplete.
FDA Determined
Cause 2		Employee error
ActionAn Urgent: Medical Device Product Correction customer notification letter, dated 4/15/2010, has been sent out to all affected accounts via regular mail in the form of a certified, return request receipt letter. Accounts will receive a follow-up phone call from a Stryker Representative to schedule a re-inspection of equipment to see if it mets established critical specifications or not. The firm recommends that customers continue using all Stryker Communications products listed in the notice. Questions can be directed to Katie Blackwell at 972-410-7660 or via email at StrykerCommunicationsRA@stryker.com.
Quantity in Commerce9
DistributionNationwide Distribution
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.
510(K) Database510(K)s with Product Code = GCJ
510(K)s with Product Code = GCJ
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