Axiom Artis model Interventional fluoroscopic x-ray foot switch accessory; Model Numbers: 4787797, 4787805, and 4787813.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Serial Numbers: 10006 10010 10017 10025 10044 10050 10051 10055 1044 1078 1081 15000 15001 15018 15021 15032 15044 15047 15056 15058 15060 15076 15088 15091 15105 15114 15116 15131 15144 15148 15149 17002 17004 17007 17011 17032 17050 17061 17062 17074 17078 17084 17142 20001 20002 20005 20009 20015 20024 20030 21004 21006 21017 21022 21028 21033 21039 21047 21052 21054 21075 21087 21089 21095 21096 21112 21114 21117 21132 21135 21150 21151 21173 21175 21178 21187 21188 21200 21201 21205 21208 21216 21225 21273 21274 21278 21281 21283 21294 21308 21309 21317 21327 21331 21337 21345 21347 21351 21352 21353 21363 21370 21377 21379 21384 21393 21400 21407 21414 21415 21421 21423 21425 21430 21440 21442 21444 21447 21448 21449 21450 21461 21462 21467 21473 21475 21484 21488 21494 21498 21500 21508 21509 21515 21519 21520 21523 21524 21536 21543 21550 21551
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Siemens Medical Solutions USA, Inc
Reason for Recall:
The possibility exists for the wireless foot switch to fail due to impacts by external factors, such as electrostatic discharge that exceed a certain intensity. If the foot switch fails, it will no longer be able to be used to release radiation. The hand switch provided can be used to release exposures; however, fluoroscopic examinations will not be possible.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Axiom Artis model Interventional fluoroscopic x-ray foot switch accessory; Model Numbers: 4787797, 4787805, and 4787813.

Product Codes/Lot Numbers:

Serial Numbers: 10006 10010 10017 10025 10044 10050 10051 10055 1044 1078 1081 15000 15001 15018 15021 15032 15044 15047 15056 15058 15060 15076 15088 15091 15105 15114 15116 15131 15144 15148 15149 17002 17004 17007 17011 17032 17050 17061 17062 17074 17078 17084 17142 20001 20002 20005 20009 20015 20024 20030 21004 21006 21017 21022 21028 21033 21039 21047 21052 21054 21075 21087 21089 21095 21096 21112 21114 21117 21132 21135 21150 21151 21173 21175 21178 21187 21188 21200 21201 21205 21208 21216 21225 21273 21274 21278 21281 21283 21294 21308 21309 21317 21327 21331 21337 21345 21347 21351 21352 21353 21363 21370 21377 21379 21384 21393 21400 21407 21414 21415 21421 21423 21425 21430 21440 21442 21444 21447 21448 21449 21450 21461 21462 21467 21473 21475 21484 21488 21494 21498 21500 21508 21509 21515 21519 21520 21523 21524 21536 21543 21550 21551

Distribution:

Nationwide distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0711-2018

Related Recalls

During patient examinations, the system may sporadically display a 0 x-ray dose administered to the patient. This behavior has only been observed during fluoroscopy and/or single-frame acquisitions. Despite the reported x-ray dose showing 0, an actual x-ray dose is applied to the patient.

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During patient examinations, the system may sporadically display a 0 x-ray dose administered to the patient. This behavior has only been observed during fluoroscopy and/or single-frame acquisitions. Despite the reported x-ray dose showing 0, an actual x-ray dose is applied to the patient.

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During 3D acquisitions, lighter and darker patient images may be captured, which may result in less accurate 3D reconstruction. The variation of brightness is a result of a constant unregulated medium dose and the angular change of patient diameter caused by rotational acquisition. This may result in unintentional low-dose radiation exposure to a patient.

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