Model Number 40KWFXPLUS, Mobile X-ray system
Pending LLM rewrite. Source: FDA_DEVICE Z-0246-2026.
Severity not yet assessed
We have not scored this recall against our rubric yet, so we are not showing a severity rating or our usual guidance. The agency’s own notice below is the authoritative source — read it first.
Plain-English summary
Sedecal sent an email to its consignees to remind the users that the equipment is not water-resistant and must be cleaned strictly according to the instructions in the manual, clearly outlining the possible consequences of improper cleaning.
The recalled product
- Product
- Model Number 40KWFXPLUS, Mobile X-ray system
- Manufacturer
- SEDECAL SA
- Category
- Medical Device — Devices
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- UDI/DI 08436046002166
- Serial Numbers: G75176
- G75504
- G76697
- G78126
- G78025
- G78715
- G78307
- G79071
- G79091
- G79193
- G80165
- G79928
- G76507
- G79861
- G80255
- G80202
- G82594
- G79057
- G73017
Distribution
Distributed in 3 states:
- CA
- IL
- NJ
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