Fabius GS Anesthesia Machine. Catalog number 8604699
FDA Recall Z-0048-2007 · Posted 2006-10-19
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Recalling FirmDraeger Medical, Inc.
Recall StatusTerminated
Product CodeBSZ
Date Initiated2006-10-03
Date Terminated2007-08-07
Product Quantity429 units
Reason for Recall
One of four casters may break loose from chassis
Firm Action
The recalling firm issued recall letters to their customers 10/03/2006 to inform them of the problem and that a service represenative will contact them to schedule an inspection of their machines. Should the inspections revealed any affected machines, the machines will be repaired free of charge.
Root Cause
Other
Distribution Pattern
Nationwide and Canada.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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