--- title: "GE OEC Medical Systems, Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search GE OEC Medical Systems, Inc recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/ge-oec-medical-systems-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # GE OEC Medical Systems, Inc recall records **9** reported ongoing 9 records in this archive. Latest source date Nov 21, 2024. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Nov 21, 2024 FDA device enforcement ### [OEC 3D REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC 3D is a mobile fluoroscopic C-Arm imaging system used to assist trained surgeons and other qualified phys...](https://isitonrecall.com/recall/fda-device-z-0703-2025-oec-3d-ref-image-intensified-fluoroscopic-x-ray-system-mobile-the-oec-3d-is-a-mobile-fluoroscopic-c/) Due to manufacturing issue of insufficient sealing of X-ray tubes and can result in a potential oil leak and loss of fluoroscopic imaging capability. Class II Reported ongoing Distribution: U.S.: AK, AZ, CA, CO, CT, DC, FL, GA, Guam, HI, IA, ID, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, W... [Official source for OEC 3D REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC 3D is a mobile fluoroscop...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0703-2025%22) Nov 21, 2024 FDA device enforcement ### [OEC Elite REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC Elite mobile C-arm is intended to provide fluoroscopic and digital spot images of the patient anatomy,...](https://isitonrecall.com/recall/fda-device-z-0704-2025-oec-elite-ref-image-intensified-fluoroscopic-x-ray-system-mobile-the-oec-elite-mobile-c-arm-is-inten/) Due to manufacturing issue of insufficient sealing of X-ray tubes and can result in a potential oil leak and loss of fluoroscopic imaging capability. Class II Reported ongoing Distribution: U.S.: AK, AZ, CA, CO, CT, DC, FL, GA, Guam, HI, IA, ID, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, W... [Official source for OEC Elite REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC Elite mobile C-arm is ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0704-2025%22) Nov 21, 2024 FDA device enforcement ### [OEC 9900 REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC 9900 Elite mobile fluoroscopy system is designed to provide fluoroscopic and spot-film images of the pa...](https://isitonrecall.com/recall/fda-device-z-0705-2025-oec-9900-ref-image-intensified-fluoroscopic-x-ray-system-mobile-the-oec-9900-elite-mobile-fluoroscop/) Due to manufacturing issue of insufficient sealing of X-ray tubes and can result in a potential oil leak and loss of fluoroscopic imaging capability. Class II Reported ongoing Distribution: U.S.: AK, AZ, CA, CO, CT, DC, FL, GA, Guam, HI, IA, ID, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, W... [Official source for OEC 9900 REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC 9900 Elite mobile fluor...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0705-2025%22) Nov 21, 2024 FDA device enforcement ### [OEC 9800 REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The Series OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic,...](https://isitonrecall.com/recall/fda-device-z-0706-2025-oec-9800-ref-image-intensified-fluoroscopic-x-ray-system-mobile-the-series-oec-9800-is-designed-to-p/) Due to manufacturing issue of insufficient sealing of X-ray tubes and can result in a potential oil leak and loss of fluoroscopic imaging capability. Class II Reported ongoing Distribution: U.S.: AK, AZ, CA, CO, CT, DC, FL, GA, Guam, HI, IA, ID, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, W... [Official source for OEC 9800 REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The Series OEC 9800 is designed...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0706-2025%22) May 15, 2023 FDA device enforcement ### [OEC Flexiview 8800 Systems with 9-inch Image Intensifier](https://isitonrecall.com/recall/fda-device-z-2275-2023-oec-flexiview-8800-systems-with-9-inch-image-intensifier/) Image intensifiers on systems, used to provide fluoroscopic/digital spot images can become detached if the systems encounter a large impact force when moved, which may result in the image intensifier falling, which could lead to injuries such as fractures, ... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of AK, 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,... [Official source for OEC Flexiview 8800 Systems with 9-inch Image Intensifier](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2275-2023%22) May 15, 2023 FDA device enforcement ### [OEC 9800 Systems with 9-inch Image Intensifier](https://isitonrecall.com/recall/fda-device-z-2276-2023-oec-9800-systems-with-9-inch-image-intensifier/) Image intensifiers on systems, used to provide fluoroscopic/digital spot images can become detached if the systems encounter a large impact force when moved, which may result in the image intensifier falling, which could lead to injuries such as fractures, ... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of AK, 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,... [Official source for OEC 9800 Systems with 9-inch Image Intensifier](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2276-2023%22) May 15, 2023 FDA device enforcement ### [OEC 9900 Systems with 9-inch Image Intensifier](https://isitonrecall.com/recall/fda-device-z-2277-2023-oec-9900-systems-with-9-inch-image-intensifier/) Image intensifiers on systems, used to provide fluoroscopic/digital spot images can become detached if the systems encounter a large impact force when moved, which may result in the image intensifier falling, which could lead to injuries such as fractures, ... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of AK, 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,... [Official source for OEC 9900 Systems with 9-inch Image Intensifier](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2277-2023%22) May 15, 2023 FDA device enforcement ### [OEC Elite Systems with 9-inch Image Intensifier](https://isitonrecall.com/recall/fda-device-z-2278-2023-oec-elite-systems-with-9-inch-image-intensifier/) Image intensifiers on systems, used to provide fluoroscopic/digital spot images can become detached if the systems encounter a large impact force when moved, which may result in the image intensifier falling, which could lead to injuries such as fractures, ... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of AK, 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,... [Official source for OEC Elite Systems with 9-inch Image Intensifier](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2278-2023%22) May 15, 2023 FDA device enforcement ### [Field Upgrade Kits: P/N 5451208 RIU, 9 INCH, TOSHIBA; P/N 5485304 SERVICE PART, IMAGE INTENSIFIER, 9 INCH, TOSHIBA; P/N 5761613 SERVICE PART, IMAGE INTENSIFIER, 9 INCH - used wi...](https://isitonrecall.com/recall/fda-device-z-2279-2023-field-upgrade-kits-p-n-5451208-riu-9-inch-toshiba-p-n-5485304-service-part-image-intensifier-9-inch/) Image intensifiers on systems, used to provide fluoroscopic/digital spot images can become detached if the systems encounter a large impact force when moved, which may result in the image intensifier falling, which could lead to injuries such as fractures, ... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of AK, 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,... [Official source for Field Upgrade Kits: P/N 5451208 RIU, 9 INCH, TOSHIBA; P/N 5485304 SERVICE PART, IMAGE INTENSIFIER...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2279-2023%22) ## Reasons in these listed records - Due to manufacturing issue of insufficient sealing of X-ray tubes and can result in a potential oil leak and loss of fluoroscopic imaging capability. - Image intensifiers on systems, used to provide fluoroscopic/digital spot images can become detached if the systems encounter a large impact force when moved, which may result in the image intensifier falling, which could lead to injuries such as fractures, hematoma, contusion,... These examples come from this result page and are not a ranking of every recall reason. ## Checking GE OEC Medical Systems, Inc ### Is there a recall on ge oec medical systems, inc right now? This archive contains 9 records, including 9 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search GE OEC Medical Systems, Inc](https://isitonrecall.com/check/?q=GE%20OEC%20Medical%20Systems%2C%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)