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FDA Medical Device Recalls (openFDA)

Siemens Medical Solutions USA, Inc: Magic View 1000U, version VE40A. Digital Image Communication System

Recall number
Z-1029-03
Recalling firm
Siemens Medical Solutions USA, Inc
Product
Magic View 1000U, version VE40A. Digital Image Communication System
Status
Terminated
Initiated
2003-02-28
Posted
2003-07-19
Terminated
2004-08-25
Reason
software issue. New examinations may not be saved properly and the examination may be lost.
Root cause
Other
Action
The recalling firm has issued a letter to their field service representative dated 2/28/02. The letter is entitled Safety Modification CN002/03/S which instructs the recalling firm's service engineers to visit each affected site and correct the software problem. A set of instructions were sent with the letter.
Quantity
49 units
Distribution
The product was shipped to medical facilities in AL, CA, CO, FL, NE, IL, IN, MI, MN, NJ, NY, OH, PA, TN, and VA.
Lot, serial or model codes
Part number 7502003
510(k) numbers
not on file
PMA numbers
not on file
Product code
not on file
Firm FEI
2240869
Firm city
Malvern
Firm state
PA
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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