SEDECAL recalls mobile x-ray systems with model SM-40HF-B-D-C; 40KW.0:002 due to not being water-resistant. Improper cleaning risks damage or safety issues. Contact SEDECAL for details.
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.
SEDEC:AL recalls specific mobile x-ray systems because they are not water-resistant. If cleaned improperly, they could be damaged or cause safety issues. Affected users should check their model numbers and contact SEDECAL for guidance.
The mobile x-ray systems are not water-resistant and must be cleaned according to the manual. Improper cleaning could lead to damage or safety issues if not followed correctly.
Users of the recalled mobile x-ray systems with model numbers SM-40HF-B-D-C; 40KW.002 are affected. Medical facilities using these systems are most at risk.
Check for model numbers SM-40HF-B-D-C; 40KW.002 on the device. Serial numbers G39544, G62558, G71736, G40116, G65568, G65570 are also affected.
Look for model number SM-40HF-B-D-C; 40KW.002 on the device.
Reach out to SEDECAL for specific guidance on proper cleaning and safety.
The mobile x-ray system is not water-resistant and must be cleaned strictly according to the manual to avoid damage or safety issues.
Model numbers SM-40HF-B-D-C; 40KW.002 with serial numbers G39544, G62558, G71736, G40116, G65568, G65570 are affected.
Check for model number SM-40HF-B-D-C; 40KW.002 or the listed serial numbers on your device.
We’ve drafted a message you can send SEDECAL to request your refund or repair — edit it as you like.
Subject: Recall Z-0278-2026 — SEDECAL SEDECAL Hello, I own a SEDECAL that is covered by recall Z-0278-2026 from SEDECAL. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
