Siemens Medical Solutions USA, Inc Siemens Primus Linear Accelerator System, PRIMART MX Linear Accelerator System; PRIMUS Mid, Part Number:1940035 and PRIMART MX, Part Number: 5500371, Siemens Medical Solutions USA, Inc., Concord, CA Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Siemens Primus Linear Accelerator System, PRIMART MX Linear Accelerator System; PRIMUS Mid, Part Number:1940035 and PRIMART MX, Part Number: 5500371, Siemens Medical Solutions USA, Inc., Concord, CA
Brand
Siemens Medical Solutions USA, Inc
Lot Codes / Batch Numbers
All Serial Numbers up to Serial Number: 3532
Products Sold
All Serial Numbers up to Serial Number: 3532
Siemens Medical Solutions USA, Inc is recalling Siemens Primus Linear Accelerator System, PRIMART MX Linear Accelerator System; PRIMUS Mid, Part Num due to Door Hinge failures; loose or falling off (Stationary Structure Doors). Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Door Hinge failures; loose or falling off (Stationary Structure Doors)
Recommended Action
Per FDA guidance
Stationary Door Hinges will be replaced on each device by the recalling firm's technician visits.
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 noticeDistribution
As reported by FDA
AL, AZ, AR, CA, CO, DE, FL, GA, ID, IL, IN, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NH, NJ, NY, NC, ND, OH, OK, PA, RI, SC, TN, TX, VA, WA, WI, DC
Page updated: Jan 10, 2026