Konica Minolta PrintLink III Model - ID/IV, code no. 0770, 0771 Medical Imaging Communication Device Model IV - product
FDA device recall Z-0220-2007 · posted 2006-11-28 · Terminated
Recall details
- Recalling firm
- Konica Minolta Medical Imaging USA, Inc.
- 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.
- Action taken
- 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
- Status
- Terminated
- Product code
- LMD
- Quantity affected
- 91 units
- Distribution
- Nationwide to imaging centers, hospitals and clinics.
- Date initiated
- 2006-10-06
- Date posted
- 2006-11-28
- Date terminated
- 2008-08-01
- Location
- Wayne, NJ
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
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| MVP (MULTI-VENDOR PROTOCOL CONVERTOR) (K900227) | Merge Technologies, Inc. | 1990-02-12 |