Reported Apr 21, 2021 · Terminated

Stryker, REF PC9001, PINPOINT Video Processor/Illuminator, Rx Only CE 0197, MD Medical Device, UDI: (01) 00858701006049…

Stryker Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Stryker Corporation · 5900 Optical Ct · San Jose, CA · 95138-1400

Is this the product you have?

  • Stryker, REF PC9001, PINPOINT Video Processor/Illuminator, Rx Only CE 0197, MD Medical Device
  • UDI(01) 00858701006049 -
  • Product Usageused with both the SPY-PHI and PINPOINT systems, the intended use for both imaging systems are being documented here
Lot codes and dates
  • 125 of 125 codes

    • PI20362910
    • PI20082806
    • PI20112868
    • PI20322887
    • PI20372920
    • PI16180922
    • PI20052735
    • PI20362908
    • PI20362911
    • PI20092807
    • PI20112869
    • PI20322888
    • PI20372921
    • PI17381211
    • PI20052740
    • PI20362909
    • PI20362913
    • PI20102835
    • PI20112870
    • PI20322889
    • PI20372922
    • PI17381214
    • PI20062759
    • PI20463033
    • PI20362912
    • PI20102836
    • PI20112871
    • PI20322890
    • PI20372923
    • PI18041369
    • PI20062766
    • PI20463038
    • PI20022723
    • PI20102839
    • PI20112872
    • PI20322891
    • PI20052734
    • PI18041410
    • PI20062768
    • PI20463041
    • PI20022724
    • PI20102846
    • PI20112873
    • PI20362892
    • PI20052736
    • PI18181490
    • PI20062771
    • PI20463042
    • PI20022725
    • PI20102851
    • PI20112874
    • PI20362893
    • PI20062747
    • PI18241579
    • PI20062772
    • PI20463046
    • PI20022726
    • PI20112852
    • PI20112875
    • PI20362894
Amount recalled
125 units

Where it was sold

Why it was recalled

Their is a potential that Video Processor/Illuminators may exhibit flickering, loss of image or unintended reboots.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Dec 15, 2023 · Data as of Sep 19, 5:45 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.