Liberty Medical Solutions recalls Multi-Mode Stimulators from 2018-2023 due to missing safety warnings in manuals. Affected units have specific serial numbers. Consumers should check if their device matches the listed serials.
The instruction manuals that were included with the Multi-Mode Stimulators distributed from 2018 to 2023 did not contain all of the appropriate warnings and contraindications.
Liberty Medical Solutions is recalling Multi-Mode Stimulators made between 2018 and 2023 because the instruction manuals did not include all necessary safety warnings and contraindications. This could lead to improper use if users rely on incomplete safety information.
The hazard comes from instruction manuals that lacked complete safety warnings and contraindications. This means users might not be aware of potential risks or conditions where the device should not be used, which could lead to improper application.
People who own or use the Multi-Mode Stimulator for medical purposes are likely affected. Those with specific serial numbers listed in the recall are most at risk.
Check if your device has a serial number listed in the provided list (e.g., 181102627, 180101759, etc.). The device was distributed from 2018 to 2023.
Compare your device's serial number with the list of affected serials provided in the recall notice.
The instruction manuals for these devices did not contain all necessary safety warnings and contraindications.
Check if your device's serial number matches the list provided in the recall notice. If it does, you may need to contact Liberty Medical Solutions for further instructions.
The recall indicates that missing safety warnings could lead to improper use, but no specific injury risks are mentioned in the notice.
We’ve drafted a message you can send Liberty Medical Solutions to request your refund or repair — edit it as you like.
Subject: Recall Z-0506-2024 — Liberty Medical Solutions Liberty Medical Solutions Hello, I own a Liberty Medical Solutions that is covered by recall Z-0506-2024 from Liberty Medical Solutions. 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.
