Draeger Medical, Inc.: Medical Device Recall in 2024 - (Recall #: Z-1512-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Dr¿ger Perseus A500 Anesthesia Workstation

Product Classification:

Class I

Date Initiated: March 20, 2024

Date Posted: April 24, 2024

Recall Number: Z-1512-2024

Event ID: 94269

Reason for Recall:

Unexpected shutdown while operating on battery power.

Status: Ongoing

Product Quantity: 16,841 units

Code Information:

Material No. MX06000; UDI-DI: 04048675253600; All Serial No.

Distribution Pattern:

Domestic: Nationwide Distribution; Foreign: Angola, Argentina, Australia, Austria, Bahrain, Belarus, Belgium, Bolivia, Botswana, Brazil, Brunei Dar-se- S, Bulgaria, Canada, Chili, China, Columbia, Costa Rica, Croatia, Czech Republic, Denmark, Ecuador, Egypt, Finland, France, French Polynesia, French Guiana, Georgia, Germany, Gibraltar, Greece, Guadeloupe, Hungary, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Kuwait, Lebanon, Liechtenstein, Lithuania, Malaysia, Maldives, Mauritius, Mayotte, Mexico, Morocco, Netherlands, New Zealand, Norway, Oman, Pakistan, Panama, Peru, Philippines, Poland, Portugal, Qatar, Reunion, Romania, Russian Federation, Saudi Arabia, Serbia, Singapore, Slovenia, Slovakia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, Turkmenistan, Uganda, Ukraine, United Kingdom, Uruguay, United Arab Emirates, Vietnam.

Voluntary or Mandated:

Voluntary: Firm initiated