Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Blue Belt Technologies Recalled by Blue Belt Technologies MN Due to Blue Belt Technologies is recalling sterile Monitor Drapes...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Blue Belt Technologies MN directly.
Affected Products
Blue Belt Technologies, Inc. Monitor Drape REF: PFSD-V0001, Rx only, Sterile EO. Product Usage: The intended use of this device is t protect equipment from contamination during a variety of procedures throughout the clinical setting.
Quantity: 60 cartons (20 pieces/carton) 40 in EU, 20 in US.
Why Was This Recalled?
Blue Belt Technologies is recalling sterile Monitor Drapes used with their Navio PFS system during orthopedic knee surgery. The drapes are used to cover the Navio PFS system computer monitor and arm assembly and provide a sterile barrier in the surgical suite. The defect is evident when the computer monitor is being draped. The front section of the drape separates from the rest of the drape at
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Blue Belt Technologies MN
Blue Belt Technologies MN has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report