Opthalmic Laser, product number 8065-5000-1
FDA device recall Z-0923-04 · posted 2004-07-20 · Terminated
Recall details
- Recalling firm
- Alcon Research, Ltd.
- Reason for recall
- Product may generate laser light flashback.
- Action taken
- Additional in-service training materials have been prepared and will be delivered to users. Additional software upgrade will be made. Actvities will be complete in May 2004.
- Root cause
- Other
- Status
- Terminated
- Product code
- HQF
- Quantity affected
- 62
- Distribution
- Nationwide and Sweden, Taiwan, Fiji Islands, Cyprus, Philippines.
- Date initiated
- 2004-04-09
- Date posted
- 2004-07-20
- Date terminated
- 2004-08-30
- Location
- Fort Worth, TX
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