Phototherapy Lamp, Model 9001W501JE
FDA device recall Z-0241-04 · posted 2003-12-18 · Terminated
Recall details
- Recalling firm
- Fisher & Paykel Healthcare Inc
- Reason for recall
- Component placement presents risk of electrocution to patients.
- Action taken
- A recall letter and a set of instructions for fixing the units was sent to customers with instructions to complete a fax back form to indicate completion of the repair.
- Root cause
- Other
- Status
- Terminated
- Product code
- LBI
- Quantity affected
- 88
- Distribution
- Nationwide.
- Date initiated
- 2003-12-05
- Date posted
- 2003-12-18
- Date terminated
- 2005-11-23
- Location
- Laguna Hills, CA
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