B-K Medical recalls ultrasound systems 1300-21 and 1300-S1 due to unclear battery replacement intervals and safety procedures in user guides.
GE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-life handling procedures, or general battery safety precautions.
B-K Medical is recalling ultrasound systems 1300-21 and 1300-S1 because the user guides don't clearly state battery replacement schedules or safety procedures. This could lead to improper battery handling.
The user guides and service manuals don't adequately describe when batteries need replacement, how to handle end-of-life batteries, or general battery safety. This could lead to improper battery handling, but the hazard is not described as causing immediate injury or death.
Healthcare professionals using these ultrasound systems at medical facilities are most at risk. The recall affects specific model numbers with serial numbers listed in the notice.
Check for model numbers 1300-21 or 1300-S1 with the serial numbers listed in the recall notice. The system includes a battery that needs regular replacement.
Check the user guide for battery replacement schedules and end-of-life procedures.
The recall states the user guides don't adequately describe battery replacement intervals and safety procedures, but it does not indicate a risk of injury or death.
Check if your system is model 1300-21 or 1300-S1 with a serial number listed in the recall notice.
Review the battery replacement instructions in the user guide. The recall does not require immediate action beyond checking the instructions.
We’ve drafted a message you can send B-K Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0436-2026 — B-K Medical B-K Medical Hello, I own a B-K Medical that is covered by recall Z-0436-2026 from B-K Medical. 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.
