Recall Z-1672-2021— Welch Allyn Inc
Class II · Terminated
Class II FDA medical device recall by Welch Allyn Inc, initiated 2021-04-22, terminated 2024-05-31. FDA's recall record names no specific 510(k) clearance for this event. Product: GS777 Wall Transformer Model: 77710 Intended Use: The GS777 Wall Transformer is intended for use in ambulatory and acute care settings.. Reason: Potential Risk of fluid ingress to the power supplies, resulting in risk of an internal electrical short and possible electrical shock.
- Recalling firm
- Welch Allyn Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2021-04-22
- Terminated
- 2024-05-31
- Firm location
- Skaneateles Falls, NY, United States
Product description
GS777 Wall Transformer Model: 77710 Intended Use: The GS777 Wall Transformer is intended for use in ambulatory and acute care settings.
Reason for recall
Potential Risk of fluid ingress to the power supplies, resulting in risk of an internal electrical short and possible electrical shock
Data sourced from openFDA. This site is unofficial and independent of the FDA.