Draeger Medical Systems recalls

Draeger Medical Systems has 12 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 5 Feb 2025. 6 are still ongoing. The most frequent reason is device malfunction.

Total recalls12since 2012
Last 12 months0reported
Class I433% of total
Ongoing6latest 5 Feb 2025

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 4 33%Class II 8 67%Class III 0 0%

Why draeger medical systems is recalled

By year

Ongoing draeger medical systems recalls

6 active

All draeger medical systems recalls, newest first

12 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIInfinity Central Station recalled by Draeger Medical SystemsDraeger Medical SystemsDevice MalfunctionNationwide
DeviceCLASS IIInfinity Acute Care System (IACS) Monitoring System recalledDraeger Medical SystemsOtherNationwide
DeviceCLASS IIDraeger Softbed Resuscitaire and/or Birthing Room Warmer recalledDraeger Medical SystemsLabeling ErrorsNationwide
DeviceCLASS IIDraeger Infinity CentralStation (ICS) recalledDraeger Medical SystemsDevice MalfunctionNationwide
DeviceCLASS IIDraeger Infinity M300 and M300+, for use recalledDraeger Medical SystemsDevice MalfunctionNationwide
DeviceCLASS IIDraeger Globe-Trotter and Globe-Trotter IC recalledDraeger Medical SystemsOtherDE, IN
DeviceCLASS IDraeger Jaundice Meter JM-105 The device is intended recalledDraeger Medical SystemsOtherNationwide
DeviceCLASS IDraeger Jaundice Meter JM-103 The device is intended recalledDraeger Medical SystemsOtherNationwide
DeviceCLASS IDraeger Oxylog 3000 plus ventilators, emergency recalledDraeger Medical SystemsDevice MalfunctionNationwide
DeviceCLASS IDraeger PS500 Power Supply Unit of the Infinity ACS recalledDraeger Medical SystemsDevice MalfunctionNationwide
DeviceCLASS IIDraeger Infinity Acute Care System Monitoring Solution recalledDraeger Medical SystemsDevice Malfunction8 states
DeviceCLASS IIDrager PT 4000 Phototherapy System recalled by Draeger Medical SystemsDraeger Medical SystemsDevice MalfunctionNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.