Konica Minolta recalls Bucky Stand SU-4000 Input units with specific serial numbers due to risk of unintended U-Arm movement during X-ray procedures.
Unintentional U-Arm movement
Konica Minolta is recalling certain Bucky Stand SU-4000 Input X-ray units because they can move unexpectedly during use. This could cause injury to patients or staff if the X-ray equipment shifts while operating.
The Bucky Stand SU-4000 Input units have a risk of unintentional U-Arm movement during X-ray procedures. This could cause the X-ray equipment to shift unexpectedly, potentially leading to injury to patients or staff if the equipment moves while in use.
Healthcare facilities using the recalled Bucky Stand SU-4000 Input units with specific serial numbers are affected. Medical staff and patients using these units during X-ray procedures are at risk of injury from unintended movement.
Check if your Bucky Stand SU-4000 Input unit has serial numbers listed in the recall notice (e.g., SU41607003 to SU41808064). These units were sold with specific firmware and board versions between November 2017 and the recall date.
Identify your unit's serial number to see if it matches the list of affected serial numbers provided in the recall notice.
The hazard is unintentional U-Arm movement during X-ray procedures, which could cause injury to patients or staff if the equipment shifts unexpectedly.
The affected serial numbers range from SU41607003 to SU41808064, as listed in the recall notice.
No, but you should check if your unit's serial number is on the list and take appropriate action if it is affected.
We’ve drafted a message you can send Konica Minolta to request your refund or repair — edit it as you like.
Subject: Recall Z-0659-2019 — Konica Minolta Konica Minolta Hello, I own a Konica Minolta that is covered by recall Z-0659-2019 from Konica Minolta. 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.
