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FDA Medical Device Recalls (openFDA)

Abbott Laboratories, Inc: AEROSET Software versions 1.00ER005, catalog number 2-89996-01 and 1.00ER005.2, catalog number 2-89996-02

Recall number
Z-0725-03
Recalling firm
Abbott Laboratories, Inc
Product
AEROSET Software versions 1.00ER005, catalog number 2-89996-01 and 1.00ER005.2, catalog number 2-89996-02
Status
Terminated
Initiated
2003-02-24
Posted
2003-04-16
Terminated
2004-10-28
Reason
Under certain operating conditions, smart wash feature disables with multiple samples.
Root cause
Other
Action
A device correction letter was sent 02/24/2003 to all AEROSET customers with a US Customer Reply Form. A Technical Service Bulletin will be released to include the Device Correction letter and instructions for Field Service Personnel. A Quality Directive will be issued to provide instructions to Customer Service.
Quantity
645 units
Distribution
Nationwide and to Mexico, Guatemala, Venezuela, Columbia, Argentina, Brazil, Puerto Rico, Dominican Republic, Canada, Germany, Hong Kong, Australia, and New Zeland
Lot, serial or model codes
No codes: Catalog numbers 2-89996-01 and 2-89996-02
510(k) numbers
["K980367"]
PMA numbers
not on file
Product code
JJE
Firm FEI
1628664
Firm city
Irving
Firm state
TX
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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