Welch Allyn recalls GS777 Wall Transformer model 77710 due to potential fluid ingress causing electrical short and shock risk. Affected units sold in ambulatory and acute care settings.
Potential Risk of fluid ingress to the power supplies, resulting in risk of an internal electrical short and possible electrical shock
Welch Allyn is recalling their GS777 Wall Transformer model 77710 because water or other fluids could enter the device, causing electrical shorts and shock. This poses a risk to users in medical settings where the device is used.
Fluids entering the power supply could cause internal electrical shorts, which may lead to electrical shock. This is particularly concerning in medical environments where devices are exposed to moisture or humidity.
Healthcare workers and patients using the GS777 Wall Transformer in ambulatory or acute care settings are most at risk. The device is designed for medical use in hospitals and clinics.
Check for the model number 77710 on the GS777 Wall Transformer. The device is intended for use in ambulatory and acute care settings, so it's likely found in hospitals and clinics.
Inspect the transformer for signs of water or fluid exposure, such as discoloration or unusual smells.
Reach out to Welch Allyn directly for guidance on whether the device needs repair or replacement.
The recall indicates potential risk of electrical shock if fluid enters the device, so it's not safe to use without checking for damage.
Look for the model number 77710 on the GS777 Wall Transformer, which is intended for use in ambulatory and acute care settings.
Contact Welch Allyn directly for guidance on whether the device needs repair or replacement.
We’ve drafted a message you can send Welch Allyn to request your refund or repair — edit it as you like.
Subject: Recall Z-1672-2021 — Welch Allyn Welch Allyn Hello, I own a Welch Allyn that is covered by recall Z-1672-2021 from Welch Allyn. 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.
