Z-0048-2007

Fabius GS Anesthesia Machine. Catalog number 8604699

Name: Z-0048-2007 Fabius GS Anesthesia Machine. Catalog number 8604699
Creator: Draeger Medical, Inc.
Published: 2006-10-03
License: https://open.fda.gov/license/

Draeger, Inc. / initiated 2006-10-03 / Terminated

FDA source

Draeger Medical, Inc. began a recall of Fabius GS Anesthesia Machine. Catalog number 8604699 on 2006-10-03. The reason FDA records is "One of four casters may break loose from chassis". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0048-2007
Status: Terminated
Initiated: 2006-10-03
Posted: 2006-10-19
Terminated: 2007-08-07
Recalling firm: Draeger, Inc.
Product: Fabius GS Anesthesia Machine. Catalog number 8604699
Product code: BSZ Gas-Machine, Anesthesia
Reason for recall: One of four casters may break loose from chassis
FDA root cause: Other
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.
Quantity in commerce: 429 units
Distribution: Nationwide and Canada.
Product codes and lots: Catalog number 8604699

Product code BSZ

K042419Class IIFabius Gs/fabius Tiro Anesthesia SystemDraeger Medical, Inc. / cleared 2004-10-08

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)