Lower riskMedical device recall · FDA · Published August 8, 2022
Stry: USB Converter Polaris Spectra Camera Recall - Infant Failures Risk
Stryker recalls USB Converter and Polaris Spectra Camera (Catalog #201148) due to potential infant failures causing non-function or error lights. Affected units may need replacement.
Certain units have the potential to exhibit infant failures whereby units either arrive non-functional, have the potential to become non-functional, or flash an error light while in use.
“Stry: USB Converter Polaris Spectra Camera Recall - Infant Failures Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/60208-stry-usb-converter-polaris-spectra-camera-recall-infant-failures-risk. Based on FDA recall #Z-1735-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1735-2022%22&limit=1).
Mako Surgical Corporation recalled Stryker USB Converters and Polaris Spectra Cameras (Catalog #201148) due to potential infant failures causing non-functionality or error lights, according to the FDA on Aug. 8, 2022.
How to tell if you have it
Brand: Stryker
Product: USB Converter, Polaris Spectra Camera
Catalog #: 201148
Lot #: 22041607
UDI-DI (GTIN): 07613327407280
Distribution: IL, AZ
The hazard
Certain units have the potential to exhibit infant failures whereby units either arrive non-functional, have the potential to become non-functional, or flash an error light while in use.
Context
GovInfoNow's records show Mako Surgical Corporation has 10 other recalls on record since June 7, 2017. Other recent recalls of similar products include Stryker XCEL Bladeless Trocar W/Optiview (Aug. 19, 2026), Olympus ShockPulse-SE Lithotripsy System Generator (Nov. 14, 2025) and Olympus ShockPulse-SE Lithotripsy System Probes (Nov. 14, 2025).
How to tell if you have this one
Check for the catalog number 201148 on the device. Units sold with lot number 22041607 or UDI-DI (GTIN) 07613327407280 are affected.
Brand
Stryker
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Device Status
Look for the catalog number 201148 on the device or lot number 22041607.
Where it went and when
Where it was distributed
Distributed in Arizona and Illinois.
Listed by the agency
Not listed
FDA distribution: “US Distribution was made to IL and AZ.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, Illinois.
Recall timeline
FDA terminated this recall 3.8 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-1735-2022 (August 8, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1735-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.