Fisher & Paykel Healthcare Inc Phototherapy Lamp, Model 9001W501JE Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Phototherapy Lamp, Model 9001W501JE
Brand
Fisher & Paykel Healthcare Inc
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
The potentially affected lamps have serial numbers within the following ranges: 2000 SN 00501XXxxxxx SN 501XXxxxxx SN 2000-501XXxxxxx 2001 SN 2001-501XXxxxxx SN 01-xx xx xxxxxx 2002 SN 02 xx xx xxxxxx 2003 SN 03 xx xx xxxxxx
Fisher & Paykel Healthcare Inc is recalling Phototherapy Lamp, Model 9001W501JE due to Component placement presents risk of electrocution to patients.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Component placement presents risk of electrocution to patients.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026