Coherent brand DUO Diode Laser Systems. A Non-medical, class IV industrial materials processing machine. The following M
FDA device recall Z-0540-04 · posted 2004-11-16 · Terminated
Recall details
- Recalling firm
- Coherent, Inc.
- Reason for recall
- Software problem that may cause unintended emission of laser radiation.
- Action taken
- On 1/19/04, the firm initiated the recall and their notification was via letters informing its customers of the corrective action.
- Root cause
- Other
- Status
- Terminated
- Product code
- L22
- Quantity affected
- 93 units
- Distribution
- 10 US customers and 6 foreign customers in Canada, Germany, Japan received this product, with 1 wholesale dealer in Amersham Health, Durham, NC.
- Date initiated
- 2004-01-19
- Date posted
- 2004-11-16
- Date terminated
- 2005-08-04
- Location
- Santa Clara, CA
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