Skip to content
Get alerts
GovInfoNow
Lower risk Medical device recall · FDA · Published April 28, 2022

GE Healthcare Centricity Radiology RA600 Software Inaccurate Measurements Recall

GE Healthcare recalls Centricity Radiology RA600 software versions 7.0-7.0 SP and 8.0-8.0 SP14H due to potential inaccurate distance and area measurements on magnified or scaled-down images. Affected units may require software update.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-1231-2022Medical deviceGE Healthcare ›
Take action

Contact the company

Recalling firmGE Healthcare, LLC3000 N Grandview Blvd · Waukesha, WI 53188-1615
✎ GovInfoNow plain-language explainer

GE Healthcare is recalling certain versions of their Centricity Radiology RA600 software because measurements on magnified or scaled-down images might be inaccurate. This could lead to incorrect medical calculations if used in radiology imaging. Affected units have specific software versions and GTIN/DI codes. Read more at govinfonow.com/recall/60752-ge-healthcare-centricity-radiology-ra600-software-inaccurate-measurements-recall.

Source Summary by GovInfoNow · govinfonow.com/recall/60752-ge-healthcare-centricity-radiology-ra600-software-inaccurate-measurements-recall · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1231-2022

Cite this page

“GE Healthcare Centricity Radiology RA600 Software Inaccurate Measurements Recall.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/60752-ge-healthcare-centricity-radiology-ra600-software-inaccurate-measurements-recall. Based on FDA recall #Z-1231-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1231-2022%22&limit=1).

GE Healthcare, LLC voluntarily recalled the Centricity Radiology RA600 on April 28, 2022, according to the FDA. The device may display inaccurate distance and area measurements on magnified or scaled-down images. Owners should contact GE Healthcare for a remedy.

How to tell if you have it

  • Brand: GE Healthcare
  • Product: Centricity Radiology RA600
  • Software Version 7.0 through 7.0 SP, No GTIN/DI (Code: 2022296-0XX)
  • Software Version 8.0 through 8.0 SP14H, GTIN/DI: 00840682125260 (Codes: 2038437-0XX, 2097190-0XX)
  • Units affected: 1,332

The hazard

The recall addresses the potential for distance and area measurements to display inaccurate values when performed on magnified images. Specific issues occur with ZFP, where measurements can be inaccurate on lossy images scaled down from their original resolution.

Context

GovInfoNow's records show GE Healthcare LLC has 97 other recalls on record since October 4, 2017. Other recent recalls of similar products include the SIGNA Premier MRI Scanners recall (February 27, 2026), the Centricity Universal Viewer 6.0/7.0/8.0 recall (July 15, 2022), and the SIGNA Premier MRI Scanner recall (June 24, 2022). Other recent recalls of similar products include the Centricity PACS Software Recall (July 31, 2026), the Centricity Universal Viewer Zero Footprint Client Recall (January 16, 2026), and the Centricity Enterprise Archive V2/V3/V4 Software Recall (July 31, 2026).

How to tell if you have this one

Check if your Centricity Radiology RA600 has software version 7.0 through 7.0 SP or 8.0 through 8.0 SP14H. Look for GTIN/DI codes 2022296-0XX or 00840682125260 with associated model codes.

  • Brand
    GE Healthcare
  • Category
    Medical device
FDA recall event · 5 products

All 5 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Ongoing
  • Distribution
    Worldwide distribution. Nationwide distribution to AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY. International distribution to Argentina, Australia, Austria, Bahamas, Belgium, Bermuda, Bolivia, Plurinational State of, Brazil, Canada, Chile, China, Colombia, Costa Rica, Denmark, Dominican Republic, Ecuador, Egypt, Finland, France, Germany, Hong Kong, Hungary, India, Indonesia, Ireland, Israel, Italy, Japan, Kazakhstan, Korea, South, Kuwait, Lebanon, Malaysia, Malta, Mexico, Namibia, Netherlands, Nigeria, Norway, Pakistan, Panama, Peru, Poland, Portugal, Puerto Rico, Qatar, Russia, Russian Federation, Saudi Arabia, Singapore, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, Trinidad And Tobago, Turkey, United Arab Emirates, United Kingdom, Uruguay, Venezuela, Bolivarian Republic of, Vietnam
Recall numberProduct, codes & lotsQuantity
Z-1229-2022Centricity Universal Viewer Zero Footprint Client; Software Version 6.0 SP11 through 6.0 SP11.4; GTIN/DI: 00840682102988; Codes: 2089507-1XX488 units
Z-1230-2022Centricity Enterprise Web; Software Versions 3.0 through 3.0 SP14d, 4.0 through 4.0 Spa6c and 4.0 Spa7b; Codes: 2027870-0XX, 2049944-0XX, 2068692-0XX.536 units
Z-1231-2022Centricity Radiology RA600; a. Software Version 7.0 through 7.0 SP, No GTIN/DI (Code: 2022296-0XX); b. Software Version 8.0 through 8.0 SP14H, GTIN/DI: 00840682125260 (Codes: 2038437-0XX, 2097190-0XX)1,332 units
Z-1232-2022Centricity Cardiology CA1000; a. Software Version 1.0 through 1.0 SP, No GTIN/DI (Code: 2022296-0XX); b. Software Version 2.0 through 2.0 SP14H, GTIN/DI: 00840682125260 (Codes: 2038437-0XX, 2097190-0XX)601 units
Z-1233-2022Centricity PACS RA1000; a. Software Version 3.0 through 3.2 SP8, No GTIN/DI (Code: 2051372-0XX, 2064678-0XX) b. Software Version 4.0 through 4.0 SP14, GTIN/DI 00840682124447 (Code: 2062264-0XX); c. 6.0 through 6.0 SP10.3, GTIN/DI: 00840682104821 (Code: 2094628-0XX); d. 7.0 through 7.0 SP0.0.4.7, GTIN/DI: 00840682145558 (Code: 5824366-0XX)676 units
Based on the official FDA remedy

What to do — step by step

  1. Check Software Version

    Verify your software version by checking the device settings or documentation for versions 7.0 through 7.0 SP or 8.0 through 8.0 SP14H.

Where it went and when

Where it was distributed

Distributed nationwide and abroad; the notice names 49 states.

Alaska: nationwideAKMaine: named in the noticeMEVermont: named in the noticeVTNew Hampshire: named in the noticeNHWashington: named in the noticeWAIdaho: named in the noticeIDMontana: named in the noticeMTNorth Dakota: named in the noticeNDMinnesota: named in the noticeMNIllinois: named in the noticeILWisconsin: named in the noticeWIMichigan: named in the noticeMINew York: named in the noticeNYRhode Island: named in the noticeRIMassachusetts: named in the noticeMAOregon: named in the noticeORNevada: named in the noticeNVWyoming: named in the noticeWYSouth Dakota: named in the noticeSDIowa: named in the noticeIAIndiana: named in the noticeINOhio: named in the noticeOHPennsylvania: named in the noticePANew Jersey: named in the noticeNJConnecticut: named in the noticeCTCalifornia: named in the noticeCAUtah: named in the noticeUTColorado: named in the noticeCONebraska: named in the noticeNEMissouri: named in the noticeMOKentucky: named in the noticeKYWest Virginia: named in the noticeWVVirginia: named in the noticeVAMaryland: named in the noticeMDDelaware: named in the noticeDEArizona: named in the noticeAZNew Mexico: named in the noticeNMKansas: named in the noticeKSArkansas: named in the noticeARTennessee: named in the noticeTNNorth Carolina: named in the noticeNCSouth Carolina: named in the noticeSCDistrict of Columbia: named in the noticeDCOklahoma: named in the noticeOKLouisiana: named in the noticeLAMississippi: named in the noticeMSAlabama: named in the noticeALGeorgia: named in the noticeGAHawaii: named in the noticeHITexas: named in the noticeTXFlorida: named in the noticeFLPuerto Rico: named in the noticePR

FDA distribution: “Worldwide distribution. Nationwide distribution to AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Alabama, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, Wyoming.

Recall timeline

FDA published this recall 48 days after the firm started it.

1. Firm started the recall: Apr 28, 202212. FDA classified it Class II: Jun 3, 202223. Published in FDA’s Enforcement Report: Jun 15, 202232022
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

Do I need to do anything if my software is not affected?

No action is needed if your software version is outside the affected ranges.

Similar recalls

Safeguard US Recalls Battle Bandages and IFAK Kits Due to Infection Risk
Safeguard US Operating LLCMiniMed Flex Insulin Pump Recall: Inaccurate Delivery Risk
Medtronic MiniMed, Inc.Medline Bariatric Rollator Recall: Detaching Wheels Risk
Medline Industries, LPCooperVision Pearle Vision 1 Day Contact Lenses: Incorrect Power Risk
CooperVision, Inc.Tandem t:slim App Recall: Pairing Issue With Abbott Sensors
Tandem Diabetes Care, Inc.

Latest medical device recalls

BMC Medical Co., Ltd. recalls BMC/REACTHEALTH Luna G3 APAP REF LG 3600
BMC Medical Co., Ltd. · July 15, 2026Medtronic MiniMed, Inc. recalls MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;
Medtr: MiniMed · July 13, 2026INTEGRATED MEDCRAFT LLC recalls Kingfisher Compact Individual First Aid Kit. REF Number: 76656. Containing the affected One-piece Guedel airway
Medcraft · July 7, 2026Pride Mobility Products Corp. recalls Brand Name: Quantum Rehab Product Name: R-TRAK Model/Catalog Number: R-TRAK Software Version: 2.0.11, new version:
Quantum Rehab · June 25, 2026ResMed Ltd. recalls Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory
ResMed · June 25, 2026Therabody, Inc recalls Charger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th Generation Theragun PRO
Therabody · June 23, 2026

Keep exploring

Where this comes from

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-1231-2022 (April 28, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1231-2022 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA