Siemens Medical Solutions USA, Inc AXIOM Sireskop SD Model numbers 8890415 and 8890407. The product is intended for use as radiographic and fluoroscopic imaging device. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
AXIOM Sireskop SD Model numbers 8890415 and 8890407. The product is intended for use as radiographic and fluoroscopic imaging device.
Brand
Siemens Medical Solutions USA, Inc
Lot Codes / Batch Numbers
Serial numbers: 51010, 71136, 51007, 51008, 71019, 71080, 71172, 71067, 41012, 71015, 71038, 71102, 71104, 71169, 51006, 51011, 51024, 51028, 71026, 71039, 71083, 71117, 71119, 41027, 71120, 71121, 41028, 71137, 71138, 71149, 71158, 71161, 71167, 71168, 71170, 51060, 71160, 51026, 71030, 71059, 71033, 71037, 41006, 51052, 51064, 71001, 71082, 71114, 71141, 71148, 71152, 71156, 51046, 71181, 51013, 51044, 71075, 71098, 51054, 71020, 71021, 71074, 71088, 41026, 71135, 71140, 71055, 71006, 71017, 71042, 71073, 71162, 71174, 41003, 51049, 71053, 71128, 71131, 41022, 71096, 71099, 71129, 51009, 51036, 51045, 71069, 71087, 71144, 41008, 71014, 71016, 71028, 71109, 71130, 71004, 71051, 71090, 71157, 51029, 51030, 51069, 71009, 71011, 71034, 71035, 71126, 71127, 71145, 51003, 51016, 71022, 71029, 71164, 51043, 51070, 71061, 71064, 71110, 71116, 51001, 51057, 41014, 71124, 71133, 51012, 51050, 71070, 71142, 71095, 41011, 51047, 71023, 71076, 71081, 71084, 51041, 41010, 71032, 41029, 71002, 71065, 71105, 71115, 51005, 71068, 51017, 51018, 51023, 71043, 71046, 41020, 71091, 71092, 71101, 71108, 71139, 71146, 71150, 71155, 71178, 51015, 51059, 51066, 71013, 71057, 71062, 71097, 41013, 71024, 41023, 71086, 51037, 71010, 71106, 71112, 51065, 51068, 71008, 41017, 71078, 41024, 71079, 71111, 71018, 71147, 51002, 71040, 41002, 51019, 51020, 41005, 51033, 41007, 51040, 51048, 51051, 51055, 51061, 71003, 71007, 71012, 41018, 71025, 41019, 71045, 71063, 71100, 71103, 71113, 71122, 71125, 71153, 71154, 71159, 71163, 71171, 71173, 71177, 51004, 51021, 51025, 51058, 71048. 71058, 71060, 71072, 41001, 51022, 51031, 51035, 51039, 71027, 71175, 51063, 71005, 71066, 71089, 71165, 71166, 71123, 71151, and 51056.
Products Sold
Serial numbers: 51010, 71136, 51007, 51008, 71019, 71080, 71172, 71067, 41012, 71015, 71038, 71102, 71104, 71169, 51006, 51011, 51024, 51028, 71026, 71039, 71083, 71117, 71119, 41027, 71120, 71121, 41028, 71137, 71138, 71149, 71158, 71161, 71167, 71168, 71170, 51060, 71160, 51026, 71030, 71059, 71033, 71037, 41006, 51052, 51064, 71001, 71082, 71114, 71141, 71148, 71152, 71156, 51046, 71181, 51013, 51044, 71075, 71098, 51054, 71020, 71021, 71074, 71088, 41026, 71135, 71140, 71055, 71006, 71017, 71042, 71073, 71162, 71174, 41003, 51049, 71053, 71128, 71131, 41022, 71096, 71099, 71129, 51009, 51036, 51045, 71069, 71087, 71144, 41008, 71014, 71016, 71028, 71109, 71130, 71004, 71051, 71090, 71157, 51029, 51030, 51069, 71009, 71011, 71034, 71035, 71126, 71127, 71145, 51003, 51016, 71022, 71029, 71164, 51043, 51070, 71061, 71064, 71110, 71116, 51001, 51057, 41014, 71124, 71133, 51012, 51050, 71070, 71142, 71095, 41011, 51047, 71023, 71076, 71081, 71084, 51041, 41010, 71032, 41029, 71002, 71065, 71105, 71115, 51005, 71068, 51017, 51018, 51023, 71043, 71046, 41020, 71091, 71092, 71101, 71108, 71139, 71146, 71150, 71155, 71178, 51015, 51059, 51066, 71013, 71057, 71062, 71097, 41013, 71024, 41023, 71086, 51037, 71010, 71106, 71112, 51065, 51068, 71008, 41017, 71078, 41024, 71079, 71111, 71018, 71147, 51002, 71040, 41002, 51019, 51020, 41005, 51033, 41007, 51040, 51048, 51051, 51055, 51061, 71003, 71007, 71012, 41018, 71025, 41019, 71045, 71063, 71100, 71103, 71113, 71122, 71125, 71153, 71154, 71159, 71163, 71171, 71173, 71177, 51004, 51021, 51025, 51058, 71048. 71058, 71060, 71072, 41001, 51022, 51031, 51035, 51039, 71027, 71175, 51063, 71005, 71066, 71089, 71165, 71166, 71123, 71151, and 51056.
Siemens Medical Solutions USA, Inc is recalling AXIOM Sireskop SD Model numbers 8890415 and 8890407. The product is intended for use as radiographi due to During interventional use and applications, the possibility exists for liquids to enter the systems.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
During interventional use and applications, the possibility exists for liquids to enter the systems.
Recommended Action
Per FDA guidance
A Customer Safety Advisory Notice dated January 8, 2009 was issued to affected customers via Update Instructions AX069/08/S. This letter informed customers of the potential issues and provided instructions to avoid its occurrence. The firm has released an Addendum to the User Manual warning of the potential hazards if liquids penetrate the systems during interventional use and applications. Direct questions about this recall to Siemens Medical Solutions USA, Inc. by calling 1-610-219-6300.
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 noticePage updated: Jan 10, 2026