Applied Medical Resources Recalls

1 recall found for Applied Medical Resources. Check if any of your products are affected.

HIGHFDA DEVICE

Applied Medical Resources Recalls Cannula Due to Blade Hazard

Applied Medical Resources recalled 450 units of the Kii Low Profile, Bladed Dual Pack on December 11, 2025, due to a potential safety issue. The blade obturator may extend beyond safe limits after assembly, posing a risk to patients. Healthcare providers and patients should stop using the device immediately.

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Brand Statistics

Total Recalls
1
Pages
1