Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stryker Recalled by Stryker Corporation Due to Their is a potential that Video Processor/Illuminators may...
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 Stryker Corporation directly.
Affected Products
Stryker, REF PC9001, PINPOINT Video Processor/Illuminator, Rx Only CE 0197, MD Medical Device, UDI: (01) 00858701006049 - Product Usage: used with both the SPY-PHI and PINPOINT systems, the intended use for both imaging systems are being documented here.
Quantity: 125 units
Why Was This Recalled?
Their is a potential that Video Processor/Illuminators may exhibit flickering, loss of image or unintended reboots.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker Corporation
Stryker Corporation has 108 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report