Konica Minolta PrintLink III Model - ID/IV, code no. 0770, 0771 Medical Imaging Communication Device Model IV - product code 5000230 Model ID, product code 5000330 Konica Minolta Medical & Graphic, Inc. No. 26-2, Nishishinjuku 1-chrome, Shinjuku-ku, Tokoyo 163-0512, Japan
FDA Recall Z-0220-2007 · Posted 2006-11-28
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Recalling FirmKonica Minolta Medical Imaging USA, Inc.
Recall StatusTerminated
Product CodeLMD
Date Initiated2006-10-06
Date Terminated2008-08-01
Product Quantity91 units
Reason for Recall
The power supply of a unit located in Japan overheated and caused a smoke condition and a small amount of flame coming off the unit.
Firm Action
Letters were sent to all customers by first class US mail, certified receipt requested on 10/10/2006. Customers were also notified by fax and e-mail and a phone call on the same day.
Root Cause
Other
Distribution Pattern
Nationwide to imaging centers, hospitals and clinics.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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