FDA Medical Device Recalls (openFDA)
Datex-Ohmeda: Multi Absorbers, reference number 8003138
- Recall number
- Z-0713-03
- Recalling firm
- Datex-Ohmeda
- Product
- Multi Absorbers, reference number 8003138
- Status
- Terminated
- Initiated
- 2003-02-12
- Posted
- 2003-04-09
- Terminated
- 2004-07-02
- Reason
- Multi Absorbers for anesthesia delivery equipment may have missing or damaged filters, exposing the patient to dust from soda lime in the absorbers.
- Root cause
- Other
- Action
- Recall letters dated February 12, 2003 requested that the product be removed from use and returned.
- Quantity
- 167 cases (6 Multi Absorbers per case)
- Distribution
- Nationwide in the United States.
- Lot, serial or model codes
- Lot numbers 728112 and 798122
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- BSF
- Firm FEI
- 2183066
- Firm city
- Madison
- Firm state
- WI
- 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