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U.S. Department of Health and Human Services

Enforcement Report - Week of July 18, 2012

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Product Detail

Product Description Drager PT 4000 Phototherapy System
Recall Number Z-1950-2012
Classification Class II
Code Info Catalog number 2M21700 and serial numbers ASCF-0037 TO ASCF-0061; ASCJ-0037 TO ASCJ-0152; ASCL-0001 TO ASCL-0025; ASCM-0001 TO ASCM-0025; and ASDA-002, 0005, 0006, 0007, 0008, 0009, 0012, 0019, 0025.
Product Distributed Qty 65
Reason For Recall A routine internal quality check found that the Drager PT 4000 Phototherapy System is fitted with a 16 Amp rated fuse instead of the specified 1.6 Amp rated fuse. This may mean that the internal fuse would not trip promptly in the event of an internal short-circuit. The possible consequence is the wall outlet circuit breaker would trip first on the device may severely overheat. There have not been any reports received from the field of such cases occurring, or any injury or harm being suffered in connection with this issue.

Event Detail

Event Id 62470
Product Type Devices
Status Ongoing
Recalling Firm Draeger Medical Systems, Inc.
City Telford
State PA
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2012-07-02
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern Nationwide Distribution-USA (nationwide) and Puerto Rico.
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