Multi Absorbers, reference number 8003138, in S/5 Aespire Start-up Kits (each containing 2 Multi Absorbers)
FDA device recall Z-0714-03 · posted 2003-04-09 · Terminated
Recall details
- Recalling firm
- Datex-Ohmeda
- Reason for recall
- Multi Absorbers for anesthesia delivery equipment may have missing or damaged filters, exposing the patient to dust from soda lime in the absorbers.
- Action taken
- Recall letters dated February 12, 2003 requested that the product be removed from use and returned.
- Root cause
- Other
- Status
- Terminated
- Product code
- BSF
- Quantity affected
- 5 S/5 Aespire Start-up kits
- Distribution
- Nationwide in the United States.
- Date initiated
- 2003-02-12
- Date posted
- 2003-04-09
- Date terminated
- 2004-07-02
- Location
- Madison, WI
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