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FDA Medical Device Recalls (openFDA)

Medical Information Technology, Inc.: MEDITECH Anatomical Pathology Software Client Releases- Client Service Releases 5.6, 5.63, 5.64, 5.65, 6.0, 6.04, 6.05, 6.06, 6.1, 6.12 and 6.13 Product Usage: Meditech Anatomical Pathology Software records, stores, codes, searches and provides reports for pathology cases. It enables pathology staff and other personnel to access related findings in real time.

Recall number
Z-1465-2012
Recalling firm
Medical Information Technology, Inc.
Product
MEDITECH Anatomical Pathology Software Client Releases- Client Service Releases 5.6, 5.63, 5.64, 5.65, 6.0, 6.04, 6.05, 6.06, 6.1, 6.12 and 6.13 Product Usage: Meditech Anatomical Pathology Software records, stores, codes, searches and provides reports for pathology cases. It enables pathology staff and other personnel to access related findings in real time.
Status
Terminated
Initiated
2012-03-30
Posted
2012-04-26
Terminated
2014-08-13
Reason
Meditech Anatomical Pathology software is being recalled because data on a pathology specimen may be inadvertently deleted.
Root cause
Software design
Action
MEDITECH sent a notification beginning on January 19, 2012 to customers who are LIVE with MEDITECH Client Server Anatomical Pathology 5.6 and higher. This notification was made via e-mailed task updates that informed customers of the software issues and the code corrections that are available.
Quantity
280
Distribution
Worldwide Distribution - USA Nationwide and the countries of Bahamas, Canada and United Kingdom.
Lot, serial or model codes
Client Service Releases 5.6, 5.63, 5.64, 5.65, 6.0, 6.04, 6.05, 6.06, 6.1, 6.12 and 6.13
510(k) numbers
not on file
PMA numbers
not on file
Product code
JQP
Firm FEI
1000120736
Firm city
Westwood
Firm state
MA
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

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

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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