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FDA Medical Device Recalls (openFDA)

Philips Medical Systems Sales & Service Region No. America: MultiDiagnost Eleva Part Numbers: 9896 001 41501 and 9896 001 41502

Recall number
Z-1307-04
Recalling firm
Philips Medical Systems Sales & Service Region No. America
Product
MultiDiagnost Eleva Part Numbers: 9896 001 41501 and 9896 001 41502
Status
Terminated
Initiated
2004-06-08
Posted
2004-08-04
Terminated
2006-02-09
Reason
When reviewing images in the module before sending them to PACS or printer the order can be erratic and out of sequence and may cause confusion with the interpretation of the examination.
Root cause
Other
Action
The firm mailed letters via certified mail to their affected customers beginning on June 8, 2004. The letters instruct their customers to modify the default display on the ViewForum to exam/series date and time until a service representative can install the upgraded software R3.2.
Quantity
8
Distribution
Philips Medical Systems North American Company distributes product to medical facilities nationwide.
Lot, serial or model codes
505039, 104530, 506247, 102666, 104136, 104838, 506155, 105194.
510(k) numbers
not on file
PMA numbers
not on file
Product code
IZI
Firm FEI
1000524572
Firm city
Bothell
Firm state
WA
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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