FDA Medical Device Recalls (openFDA)
Abbott Laboratories, Inc: AEROSET Analyzer, Systems Operation Manual.
- Recall number
- Z-0016-05
- Recalling firm
- Abbott Laboratories, Inc
- Product
- AEROSET Analyzer, Systems Operation Manual.
- Status
- Terminated
- Initiated
- 2004-09-24
- Posted
- 2004-10-09
- Terminated
- 2005-11-03
- Reason
- Changes to the printer default settings made by users/operators cause printed data to be truncated and misidentified.
- Root cause
- Other
- Action
- The recall was initiated by Device Correction Letter to all AEROSET customers. The Device Correction Letter will be provided to new customers until the new revision of the Operations Manual.
- Quantity
- 835 units
- Distribution
- Nationwide and to: Mexico, Columbia, Puerto Rico, Germany, New Zealand, Guatemala, Argentina, Dominican Republic, Hong Kong, Romania, Venezuela, Brazil, Canada, and Australia
- Lot, serial or model codes
- All Systems Operations Manuals
- 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