What the US Food and Drug Administration has cleared, approved and recalled on this topic, and the side effects people report.
Each number has its full source under its own list below.
7 recalls (since 1 Jan 2023). Recalls of medical devices for this topic, newest first.
Reason: Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Reason: Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Reason: Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Reason: Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
Reason: Potential for exoskeleton to lose lateral balance and cause patient to fall.
Reason: Due to incorrect milled titanium abutment being packaged and labeled.
Reason: Due to walkers not meeting product specifications. Walkers were manufactured with misaligned wheels.
Source: openFDA, Medical device recalls, since 1 Jan 2023. Retrieved 12 Nov 2026.
3 devices cleared (since 1 Jan 2023). Devices the FDA cleared to sell in the US, newest first.
Company: Shenzhen Changkun Technology Co., Ltd.
Company: The ScottCare Corporation
Company: Shenzhen Zuowei Technology Co., Ltd.
Source: openFDA, Premarket notifications (510(k)) cleared, since 1 Jan 2023. Retrieved 12 Nov 2026.
Worldwide · 2024–2034
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View report Healthcare ServicesWorldwide · 2024–2034
View report Public HealthWorldwide · 2024–2034
View report Public HealthWorldwide · 2024–2034
View report Medical DevicesWorldwide · 2024–2034
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