Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Drager PT 4000 Phototherapy System Recalled by Draeger Medical Systems, Inc. Due to A routine internal quality check found that the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Draeger Medical Systems, Inc. directly.
Affected Products
Drager PT 4000 Phototherapy System
Quantity: 65
Why Was This Recalled?
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 b
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Draeger Medical Systems, Inc.
Draeger Medical Systems, Inc. has 12 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report