--- title: "Invacare Corporation Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Invacare Corporation recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/invacare-corporation/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Invacare Corporation recall records **7** reported ongoing 7 records in this archive. Latest source date Jan 22, 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 Jan 22, 2024 FDA device enforcement ### [Invacare Homecare Series Bed and Invacare G-Series Beds Containing Component Model Numbers: (1) G50 (2) G53 (3) G54 (4) BAR5490IVC (5) BAR5000IVC (6) 5000IVC (7) 5490IVC (8) 549...](https://isitonrecall.com/recall/fda-device-z-1251-2024-invacare-homecare-series-bed-and-invacare-g-series-beds-containing-component-model-numbers-1-g50-2-g/) Invacare Homecare & G-Series Bed Components identified with a potential weld defect leads to premature weld failures to occur on these components Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for Invacare Homecare Series Bed and Invacare G-Series Beds Containing Component Model Numbers: (1) G...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1251-2024%22) Jun 15, 2023 FDA device enforcement ### [DOLOMITE GLOSS ROLLATOR - intended to support during walking and may also serve as a resting seat. Model Number(s): 1654807 - DOLOMITE GLOSS 680 ROLLATOR 1655081 - DOLOMITE GLOS...](https://isitonrecall.com/recall/fda-device-z-2445-2023-dolomite-gloss-rollator-intended-to-support-during-walking-and-may-also-serve-as-a-resting-seat-mode/) Premature failure of the seat during use, the plastic eyelets of the folding mechanism of the device's seat can break, and in a worst-case crossbar also breaks and the Rollator can collapse causing injury to user Class II Reported ongoing Distribution: US Nationwide distribution. [Official source for DOLOMITE GLOSS ROLLATOR - intended to support during walking and may also serve as a resting seat...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2445-2023%22) Jun 10, 2022 FDA device enforcement ### [Invacare Platinum 5NXG Oxygen Concentrator, Model Numbers P5NXG1, P5NXGC1 (Canada specific model)](https://isitonrecall.com/recall/fda-device-z-1369-2022-invacare-platinum-5nxg-oxygen-concentrator-model-numbers-p5nxg1-p5nxgc1-canada-specific-model/) Between March 2, 2021 and December 31, 2021, the product label used in production did not contain the "Rx Only" statement as required. Class III Reported ongoing Distribution: Domestic distribution to the following states: ALASKA ARIZONA CALIFORNIA COLORADO GEORGIA IDAHO IOWA KANSAS KENTUCKY MICHIGAN MINNESOTA MISSOURI NEW YORK NORTH CAROLINA OHIO OKL... [Official source for Invacare Platinum 5NXG Oxygen Concentrator, Model Numbers P5NXG1, P5NXGC1 (Canada specific model)](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1369-2022%22) Mar 30, 2022 FDA device enforcement ### [Invacare TDX SP2, Model Nos. TDXSP2 TDXSP2-MCG TDXSP2V](https://isitonrecall.com/recall/fda-device-z-1130-2022-invacare-tdx-sp2-model-nos-tdxsp2-tdxsp2-mcg-tdxsp2v/) The battery wiring harness on affected wheelchairs may become disconnected during shipment from the factory or during wheelchair use traversing large obstacles or after a jolt or impact to the wheelchair. The disconnection of the battery harness results in ... Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide distribution in the states of AK, AR, CA, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NJ, NY, OH, OR, ... [Official source for Invacare TDX SP2, Model Nos. TDXSP2 TDXSP2-MCG TDXSP2V](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1130-2022%22) Nov 12, 2021 FDA device enforcement ### [Invacare TDX SP2 with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: TDX SP2: TDXSP2, TDXSP2-CG, TDXSP2X-CG, TDXSP2-MCG, ...](https://isitonrecall.com/recall/fda-device-z-0445-2022-invacare-tdx-sp2-with-linx-gyro-power-wheelchair-with-linx-gyro-module-model-numbers-dlx-gry100-a-an/) Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2 can experience a more aggressive deceleration rate than the programmed rate due to the system following the incorrect deceleration profile, resulting in potential injury Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Australia, Thailand, New Zealand. [Official source for Invacare TDX SP2 with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0445-2022%22) Nov 12, 2021 FDA device enforcement ### [Invacare AVIVA FX with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: IFX-20R, IFX-20SP, IFX-20MP, IFX-20C](https://isitonrecall.com/recall/fda-device-z-0446-2022-invacare-aviva-fx-with-linx-gyro-power-wheelchair-with-linx-gyro-module-model-numbers-dlx-gry100-a-a/) Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2 can experience a more aggressive deceleration rate than the programmed rate due to the system following the incorrect deceleration profile, resulting in potential injury Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Australia, Thailand, New Zealand. [Official source for Invacare AVIVA FX with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0446-2022%22) Nov 12, 2021 FDA device enforcement ### [Invacare AVIVA Storm RX with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-GRY100-A and DLX-GRY101-A) Models: SRX-20R, SRX-20SP, SRX-20MP](https://isitonrecall.com/recall/fda-device-z-0447-2022-invacare-aviva-storm-rx-with-linx-gyro-power-wheelchair-with-linx-gyro-module-model-numbers-dlx-gry1/) Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2 can experience a more aggressive deceleration rate than the programmed rate due to the system following the incorrect deceleration profile, resulting in potential injury Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Canada, Australia, Thailand, New Zealand. [Official source for Invacare AVIVA Storm RX with LiNX Gyro Power Wheelchair (with LiNX Gyro Module Model Numbers DLX-...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0447-2022%22) ## Reasons in these listed records - Invacare Homecare & G-Series Bed Components identified with a potential weld defect leads to premature weld failures to occur on these components - Premature failure of the seat during use, the plastic eyelets of the folding mechanism of the device's seat can break, and in a worst-case crossbar also breaks and the Rollator can collapse causing injury to user - Between March 2, 2021 and December 31, 2021, the product label used in production did not contain the "Rx Only" statement as required. - The battery wiring harness on affected wheelchairs may become disconnected during shipment from the factory or during wheelchair use traversing large obstacles or after a jolt or impact to the wheelchair. The disconnection of the battery harness results in loss of power to the... These examples come from this result page and are not a ranking of every recall reason. ## Checking Invacare Corporation ### Is there a recall on invacare corporation right now? This archive contains 7 records, including 7 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 Invacare Corporation](https://isitonrecall.com/check/?q=Invacare%20Corporation) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)