Medical Device Recall: Z-0016-05

FDA Recalls dataset · Firm: Abbott Laboratories, Inc · Status: Terminated

Recall Action Class: N/A Date Initiated: 2004-09-24 Recall record compiled from public FDA source records.

Recall Parameters & Description

Normalized public record details for FDA recall code Z-0016-05.

Recall Res Number
Z-0016-05
Recalling Firm / Manufacturer
FEI Number
1628664
Recall Status
Terminated
Recall Classification
N/A
Date Initiated
2004-09-24
Date Posted
2004-10-09
Date Terminated
2005-11-03
Product Code
JJE
Event Number
30114
Product Quantity
835 units
Product Description AEROSET Analyzer, Systems Operation Manual.

Reason for Recall Changes to the printer default settings made by users/operators cause printed data to be truncated and misidentified.

Action Details 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.

Distribution Pattern Nationwide and to: Mexico, Columbia, Puerto Rico, Germany, New Zealand, Guatemala, Argentina, Dominican Republic, Hong Kong, Romania, Venezuela, Brazil, Canada, and Australia

Code Information / Serial Numbers All Systems Operations Manuals

Related Establishments / Registrations

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This page represents an index of public-record FDA device recalls. It does not imply current safety or compliance status of the product. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Refer to official government sources for primary safety alerts.

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