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FDA Medical Device Recalls (openFDA)

BD Biosciences, Systems & Reagents: CellQuest Pro SW, version 4.0.2. and later; Becton Dickinson, San Jose, CA 95131 CellQuest Pro software allows you to acquire and analyze data from your flow cytometer on a Macintosh computer.

Recall number
Z-1845-2011
Recalling firm
BD Biosciences, Systems & Reagents
Product
CellQuest Pro SW, version 4.0.2. and later; Becton Dickinson, San Jose, CA 95131 CellQuest Pro software allows you to acquire and analyze data from your flow cytometer on a Macintosh computer.
Status
Terminated
Initiated
2007-09-07
Posted
2011-03-30
Terminated
2011-03-31
Reason
Results and gates could be mismatched if you utilize the undo function to undo a gate that was deleted.
Root cause
Software design
Action
Important Product Information letters, dated September 2007, were sent the week of 9/14/2001 via Federal Express to all affected customers. The letters identified the affected product along with the reason for recall. The letter states that "as long as customers do not use the Undo function to undo a gate deletion, the software can be used with full functionality." The letter also states that BD will change the issue in the next software version. If customers believe that they may have analyzed sample files by utilizing the Undo function, then it is recommended that the sample files be re-analyzed. If customers need more information they should contact the Customer Support Center at 877-232-8995.
Quantity
4552
Distribution
Worldwide Distribution
Lot, serial or model codes
Catalog numbers: 343926, 339455, 343928, 347527, and 347526.
510(k) numbers
["K946055"]
PMA numbers
not on file
Product code
GKZ
Firm FEI
2916837
Firm city
San Jose
Firm state
CA
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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