Stryker, REF PC9001, PINPOINT Video Processor/Illuminator, Rx Only CE 0197, MD Medical Device, UDI: (01)…
Medical device recall Z-1428-2021. Published in FDA’s Enforcement Report on Apr 21, 2021.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Apr 21, 2021. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Nationwide FDA’s word, and 17 states named
- 125 units how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
Their is a potential that Video Processor/Illuminators may exhibit flickering, loss of image or unintended reboots.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
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.
125 units, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
PI20362910 PI20082806 PI20112868 PI20322887 PI20372920 PI16180922 PI20052735 PI20362908 PI20362911 PI20092807 PI20112869 PI20322888 PI20372921 PI17381211 PI20052740 PI20362909 PI20362913 PI20102835 PI20112870 PI20322889 PI20372922…
Every code shown here, 1,374 characters
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 PI20062754 PI19182075 PI20072773 PI20463049 PI20062749 PI20112860 PI20112876 PI20362895 PI20082802 PI19182080 PI20072780 PI20463051 PI20082795 PI20112861 PI20282879 PI20362896 PI20092808 PI19242192 PI20072781 PI20463052 PI20082797 PI20112862 PI20282880 PI20372914 PI20022701 PI19342372 PI20072784 PI20463054 PI20082798 PI20112863 PI20312881 PI20372915 PI20082788 PI19372413 PI20072787 PI20463058 PI20082799 PI20112864 PI20312882 PI20372916 PI20463062 PI19432511 PI20362904 PI20463036 PI20082801 PI20112865 PI20312883 PI20372917 PI14350291 PI20052727 PI20362905 PI20082804 PI20112866 PI20322885 PI20372918 PI15150533 PI20052728 PI20362906 PI20082805 PI20112867 PI20322886 PI20372919 PI15240575 PI20052732 PI20362907
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
Worldwide distribution - US Nationwide distribution including in the states of CA, CO, FL, IL, MA MI, MS NC, NV, OK, PA, SC, TN, TX, VA, WA, WI and the countries of AE, CA, CN, CZ, DE, ES, HK, JP, KR, KW, MX, MY, PH, RO, SG, TR, TW.
The states and territories these words name
17 states and territories.
Every one of them
- California
- Colorado
- Florida
- Illinois
- Massachusetts
- Michigan
- Mississippi
- North Carolina
- Nevada
- Oklahoma
- Pennsylvania
- South Carolina
- Tennessee
- Texas
- Virginia
- Washington
- Wisconsin
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
The words say it went outside the United States too.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Feb 26, 2021.
- FDA classified it on Apr 15, 2021.
- FDA’s Enforcement Report published it on Apr 21, 2021.
- FDA terminated it on Dec 15, 2023.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Stryker Corporation, of San Jose, CA.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.