Abbott Laboratories, Inc AEROSET Analyzer, Systems Operation Manual. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
AEROSET Analyzer, Systems Operation Manual.
Brand
Abbott Laboratories, Inc
Lot Codes / Batch Numbers
All Systems Operations Manuals
Products Sold
All Systems Operations Manuals
Abbott Laboratories, Inc is recalling AEROSET Analyzer, Systems Operation Manual. due to Changes to the printer default settings made by users/operators cause printed data to be truncated and misidentified.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Changes to the printer default settings made by users/operators cause printed data to be truncated and misidentified.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026