Konica Minolta recalls Sonimage HS1 Ultrasound Kit AC adapters with Product Number A7AP that may break internally, causing smoke emission. Affected units have specific serial numbers starting with 'A7AP-'.
There is a risk of circuit board breakage within the main housing of the AC Adapter unit. Smoke may be emitted from the AC Adapter as a direct result.
Konica Minolta is recalling Sonimage HS1 Ultrasound Kit AC adapters that could break internally, potentially emitting smoke. This poses a fire risk if the adapter is used normally.
The AC adapter's internal circuit board may break, leading to smoke emission. This could cause a fire hazard if the adapter is used normally, especially in medical settings where equipment is critical.
Medical professionals using the Sonimage HS1 ultrasound system are most at risk. The recall affects specific AC adapters with Product Number A7AP and serial numbers starting with 'A7AP-'.
Check if your Sonimage HS1 ultrasound system's AC adapter has Product Number A7AP. Serial numbers start with 'A7AP-' and include the listed numbers (e.g., 00045, 00041, etc.).
Look for a serial number starting with 'A7AP-' on the adapter's label.
If your adapter has a serial number from the list, stop using it immediately to prevent smoke emission.
The AC adapter may break internally, causing smoke emission which could lead to a fire hazard.
Serial numbers starting with 'A7AP-' and listed in the recall (e.g., 00045, 00041, etc.).
The recall does not specify a return process, but you should stop using it if it has an affected serial number.
We’ve drafted a message you can send Konica Minolta to request your refund or repair — edit it as you like.
Subject: Recall Z-1212-2018 — Konica Minolta Konica Minolta Hello, I own a Konica Minolta that is covered by recall Z-1212-2018 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.
