3 Series Full Body Phototherapy Device with Smart Touch Control System, Models #PASNBSM-2424.
FDA device recall Z-1233-04 · posted 2004-07-30 · Terminated
Recall details
- Recalling firm
- Daavlin Distributing Company
- Reason for recall
- Software errors cause the unit to not deliver the prescribed therapy and do not allow the patient records to be saved.
- Action taken
- The firm has software patches to correct the programming problems as they are reported by the users. These patches are being installed either by a service representative for the manufacturer or by the customer
- Root cause
- Other
- Status
- Terminated
- Product code
- FTC
- Quantity affected
- 2 units distributed domestically.
- Distribution
- Nation wide plus Canada, the Philippines, Saudi Arabia, Turkey & Germany
- Date initiated
- 2003-09-01
- Date posted
- 2004-07-30
- Date terminated
- 2007-07-24
- Location
- Bryan, OH
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