Atlas FDA

Extron Electronics OEM, CAB, DVI-I to DVI (3ft.); Part #: 43-112-01 (Stryker Part #: 0100-224-108); Distributed by Stryk

FDA device recall Z-0303-2008 · posted 2008-01-12 · Terminated

Recall details

Recalling firm
Stryker Communications
Reason for recall
Intermitten or Complete Loss of Signal: out-of-specification DVI cables causing intermitten or complete loss of signal on monitors used in surgery.
Action taken
Firm notified consignees of recall via letter (Urgent Device Recall) on 09/21/07. Consignees were notified that a customer service representative would visit each facility to replace out-of-spec cables with properly shielded cables at no charge.
Root cause
Nonconforming Material/Component
Status
Terminated
Product code
GCJ
Quantity affected
1,653 cables.
Distribution
Worldwide: USA and Australia, Belgium, Canada, France, Germany, Great Britain, Hong Kong, Japan, Korea, Mexico, Netherlands, New Zealand, Portugal, South Africa, Spain, Sweden, Switzerland, Taiwan, an
Date initiated
2007-10-03
Date posted
2008-01-12
Date terminated
2008-06-16
Location
Flower Mound, TX

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