Anestar Anesthesia Delivery System
FDA device recall Z-1441-04 · posted 2004-09-09 · Terminated
Recall details
- Recalling firm
- Datascope Corp
- Reason for recall
- Failure of the Anestar AC Main Power Switch. Battery should last 30 minutes, then ventilation and monitoring will fail.
- Action taken
- A Field Correction action was initiated in June, 2003 and completed by the service reps in April, 2004.
- Root cause
- Other
- Status
- Terminated
- Product code
- BSZ
- Distribution
- The units were distributed to 29 hospitals nationwide. There are no US Government military or civilian customers.
- Date initiated
- 2003-06-24
- Date posted
- 2004-09-09
- Date terminated
- 2006-10-03
- Location
- Mahwah, NJ
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