Reported Jan 25, 2023 · Ongoing
AXIOM Luminos TF, AXIOM Iconos R100, AXIOM Iconos R200 and AXIOM Luminos dRF
Siemens Medical Solutions USA, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Siemens Medical Solutions USA, Inc · 40 Liberty Blvd · Malvern, PA · 19355-1418
Is this the product you have?
AXIOM Luminos TFAXIOM Iconos R100AXIOM Iconos R200 and AXIOM Luminos dRF
- Lot codes and dates
5 of 5 products
Products covered by this recall # Product as published 1 AXIOM Luminos TF, Material #10093902 (no UDI) 2 AXIOM Iconos R100, Material #05895151 (no UDI) 3 AXIOM Iconos R200 C69, Material #10093961 (no UDI) 4 AXIOM Iconos R200 C20, Material #10093962 (no UDI) 5 AXIOM Luminos dRF, Material #10094200 (no UDI) - Amount recalled
- 654 units
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Why it was recalled
There is potential for the footrest to detach from the patient table during use.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Siemens Medical Solutions USA, Inc. recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.