--- title: "Getinge Usa Sales Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Getinge Usa Sales 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/getinge-usa-sales-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Getinge Usa Sales Inc recall records **46** reported ongoing 48 records in this archive. Latest source date Jan 15, 2025. 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 15, 2025 FDA device enforcement ### [Vaporizer Sevoflurane, Quik-Fil. Model Number: 6682285. Device is a component of Flow-i C20, Flow-i C30, Flow-i C40, Flow-c, Flow-e. For use during anesthesia.](https://isitonrecall.com/recall/fda-device-z-1074-2025-vaporizer-sevoflurane-quik-fil-model-number-6682285-device-is-a-component-of-flow-i-c20-flow-i-c30-f/) Sevoflurane used with the vaporizer may degrade to hydrogen fluoride, which could present a risk to patients or health care providers through inhalation and/or skin exposure. Potential harms include irritation of respiratory tract, which in worst case may l... Class I Reported ongoing Distribution: Domestic distribution to Kentucky and Connecticut. [Official source for Vaporizer Sevoflurane, Quik-Fil. Model Number: 6682285. Device is a component of Flow-i C20, Flow...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1074-2025%22) Oct 3, 2024 FDA device enforcement ### [MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examinati...](https://isitonrecall.com/recall/fda-device-z-0456-2025-meera-cl-mobile-operating-table-designed-for-the-placement-and-positioning-of-the-patient-immediatel/) Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Bhutan, Brazil, Canada, Chile, Colombia, Costa Rica, Croatia, Czech Republic, Ecuador, Egypt, Fra... [Official source for MEERA CL mobile operating table - Designed for the placement and positioning of the patient immed...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0456-2025%22) Oct 3, 2024 FDA device enforcement ### [MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examinati...](https://isitonrecall.com/recall/fda-device-z-0457-2025-meera-cl-mobile-operating-table-designed-for-the-placement-and-positioning-of-the-patient-immediatel/) Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Bhutan, Brazil, Canada, Chile, Colombia, Costa Rica, Croatia, Czech Republic, Ecuador, Egypt, Fra... [Official source for MEERA CL mobile operating table - Designed for the placement and positioning of the patient immed...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0457-2025%22) Oct 3, 2024 FDA device enforcement ### [MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examinati...](https://isitonrecall.com/recall/fda-device-z-0458-2025-meera-cl-mobile-operating-table-designed-for-the-placement-and-positioning-of-the-patient-immediatel/) Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Bhutan, Brazil, Canada, Chile, Colombia, Costa Rica, Croatia, Czech Republic, Ecuador, Egypt, Fra... [Official source for MEERA CL mobile operating table - Designed for the placement and positioning of the patient immed...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0458-2025%22) Oct 3, 2024 FDA device enforcement ### [MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examinati...](https://isitonrecall.com/recall/fda-device-z-0459-2025-meera-cl-mobile-operating-table-designed-for-the-placement-and-positioning-of-the-patient-immediatel/) Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Bhutan, Brazil, Canada, Chile, Colombia, Costa Rica, Croatia, Czech Republic, Ecuador, Egypt, Fra... [Official source for MEERA CL mobile operating table - Designed for the placement and positioning of the patient immed...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0459-2025%22) Oct 3, 2024 FDA device enforcement ### [MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examinati...](https://isitonrecall.com/recall/fda-device-z-0460-2025-meera-cl-mobile-operating-table-designed-for-the-placement-and-positioning-of-the-patient-immediatel/) Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Bhutan, Brazil, Canada, Chile, Colombia, Costa Rica, Croatia, Czech Republic, Ecuador, Egypt, Fra... [Official source for MEERA CL mobile operating table - Designed for the placement and positioning of the patient immed...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0460-2025%22) Oct 3, 2024 FDA device enforcement ### [MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examinati...](https://isitonrecall.com/recall/fda-device-z-0461-2025-meera-cl-mobile-operating-table-designed-for-the-placement-and-positioning-of-the-patient-immediatel/) Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Bhutan, Brazil, Canada, Chile, Colombia, Costa Rica, Croatia, Czech Republic, Ecuador, Egypt, Fra... [Official source for MEERA CL mobile operating table - Designed for the placement and positioning of the patient immed...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0461-2025%22) Oct 3, 2024 FDA device enforcement ### [MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examinati...](https://isitonrecall.com/recall/fda-device-z-0462-2025-meera-cl-mobile-operating-table-designed-for-the-placement-and-positioning-of-the-patient-immediatel/) Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Bhutan, Brazil, Canada, Chile, Colombia, Costa Rica, Croatia, Czech Republic, Ecuador, Egypt, Fra... [Official source for MEERA CL mobile operating table - Designed for the placement and positioning of the patient immed...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0462-2025%22) Oct 3, 2024 FDA device enforcement ### [MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examinati...](https://isitonrecall.com/recall/fda-device-z-0463-2025-meera-cl-mobile-operating-table-designed-for-the-placement-and-positioning-of-the-patient-immediatel/) Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Bhutan, Brazil, Canada, Chile, Colombia, Costa Rica, Croatia, Czech Republic, Ecuador, Egypt, Fra... [Official source for MEERA CL mobile operating table - Designed for the placement and positioning of the patient immed...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0463-2025%22) May 29, 2024 FDA device enforcement ### [ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322B4](https://isitonrecall.com/recall/fda-device-z-2271-2024-alphamaxx-mobile-operating-table-model-number-part-number-113322b4/) The recall is prompted by a defective charger unit (0970.2873) for models 1133.22B4, 1133.22B5, and 1133.22F5 of the ALPHAMAXX mobile operating table. This issue poses a risk of inadequate charging and operational failure. Class II Reported ongoing Distribution: Domestic: KY, NC, NY, VA. International: Australia, Bulgaria, Croatia, Czech Republic, Denmark, France, Greece, Hong Kong, Ireland, Israel, Japan, Jordan, Kuwait, Mexico, New Ze... [Official source for ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322B4](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2271-2024%22) May 29, 2024 FDA device enforcement ### [ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322B5](https://isitonrecall.com/recall/fda-device-z-2272-2024-alphamaxx-mobile-operating-table-model-number-part-number-113322b5/) The recall is prompted by a defective charger unit (0970.2873) for models 1133.22B4, 1133.22B5, and 1133.22F5 of the ALPHAMAXX mobile operating table. This issue poses a risk of inadequate charging and operational failure. Class II Reported ongoing Distribution: Domestic: KY, NC, NY, VA. International: Australia, Bulgaria, Croatia, Czech Republic, Denmark, France, Greece, Hong Kong, Ireland, Israel, Japan, Jordan, Kuwait, Mexico, New Ze... [Official source for ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322B5](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2272-2024%22) May 29, 2024 FDA device enforcement ### [ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322F5](https://isitonrecall.com/recall/fda-device-z-2273-2024-alphamaxx-mobile-operating-table-model-number-part-number-113322f5/) The recall is prompted by a defective charger unit (0970.2873) for models 1133.22B4, 1133.22B5, and 1133.22F5 of the ALPHAMAXX mobile operating table. This issue poses a risk of inadequate charging and operational failure. Class II Reported ongoing Distribution: Domestic: KY, NC, NY, VA. International: Australia, Bulgaria, Croatia, Czech Republic, Denmark, France, Greece, Hong Kong, Ireland, Israel, Japan, Jordan, Kuwait, Mexico, New Ze... [Official source for ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322F5](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2273-2024%22) May 1, 2024 FDA device enforcement ### [Vaporizer Sevoflurane Maquet Filling, Product code/REF number (6682282), Component of: Flow-i C20, Flow-i C30,Flow-i C40, Flow-c, Flow-e.](https://isitonrecall.com/recall/fda-device-z-1877-2024-vaporizer-sevoflurane-maquet-filling-product-code-ref-number-6682282-component-of-flow-i-c20-flow-i/) Sevoflurane used with the vaporizer may degrade to hydrogen fluoride, which could present a risk to patients or health care providers through inhalation and/or skin exposure. Potential harms include irritation of respiratory tract, which in worst case may l... Class I Reported ongoing Distribution: Domestic: CA, CO, IN, MO, OR, VA, WA. International: Aruba, Australia, Austria, Belgium, Bolivia, Bosnia-Herzegovina, Brazil, Bulgaria, Chile, China, Costa Rica, Czech Republic,... [Official source for Vaporizer Sevoflurane Maquet Filling, Product code/REF number (6682282), Component of: Flow-i C20...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1877-2024%22) Dec 11, 2023 FDA device enforcement ### [Flow-i C20 Anesthesia System, model 6677200](https://isitonrecall.com/recall/fda-device-z-0987-2024-flow-i-c20-anesthesia-system-model-6677200/) Potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any of which could lead to a hazardous situation. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, DC, FL, GA, IN, MA, MI, MO, NY, OH, OR, PA, TX, VA, WA & WV. [Official source for Flow-i C20 Anesthesia System, model 6677200](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0987-2024%22) Dec 11, 2023 FDA device enforcement ### [Flow-i C30 Anesthesia System, model 6677300](https://isitonrecall.com/recall/fda-device-z-0988-2024-flow-i-c30-anesthesia-system-model-6677300/) Potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any of which could lead to a hazardous situation. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, DC, FL, GA, IN, MA, MI, MO, NY, OH, OR, PA, TX, VA, WA & WV. [Official source for Flow-i C30 Anesthesia System, model 6677300](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0988-2024%22) Dec 11, 2023 FDA device enforcement ### [Flow-i C40 Anesthesia System, model 6677400](https://isitonrecall.com/recall/fda-device-z-0989-2024-flow-i-c40-anesthesia-system-model-6677400/) Potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any of which could lead to a hazardous situation. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, DC, FL, GA, IN, MA, MI, MO, NY, OH, OR, PA, TX, VA, WA & WV. [Official source for Flow-i C40 Anesthesia System, model 6677400](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0989-2024%22) Dec 11, 2023 FDA device enforcement ### [Flow-c Anesthesia System, model 6887700](https://isitonrecall.com/recall/fda-device-z-0990-2024-flow-c-anesthesia-system-model-6887700/) Potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any of which could lead to a hazardous situation. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, DC, FL, GA, IN, MA, MI, MO, NY, OH, OR, PA, TX, VA, WA & WV. [Official source for Flow-c Anesthesia System, model 6887700](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0990-2024%22) Dec 11, 2023 FDA device enforcement ### [Flow-e Anesthesia System, model 6887900](https://isitonrecall.com/recall/fda-device-z-0991-2024-flow-e-anesthesia-system-model-6887900/) Potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any of which could lead to a hazardous situation. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, DC, FL, GA, IN, MA, MI, MO, NY, OH, OR, PA, TX, VA, WA & WV. [Official source for Flow-e Anesthesia System, model 6887900](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0991-2024%22) Nov 8, 2023 FDA device enforcement ### [Maquet PowerLEDII OR Light System, Model Names and Catalog Numbers PWDII77SF - ARDPWT629100A, PWDII555DF - ARDPWT629101A, PWDII555SF - ARDPWT629102A, PWDII755DF - ARDPWT629103A,...](https://isitonrecall.com/recall/fda-device-z-0757-2024-maquet-powerledii-or-light-system-model-names-and-catalog-numbers-pwdii77sf-ardpwt629100a-pwdii555df/) A potential for a light system to fall in the operating room. Class II Reported ongoing Distribution: US Nationwide. Global Distribution. [Official source for Maquet PowerLEDII OR Light System, Model Names and Catalog Numbers PWDII77SF - ARDPWT629100A, PWD...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0757-2024%22) Nov 8, 2023 FDA device enforcement ### [Maquet Volista, Volista Access, Volista Access II, Volista Standop OR Light System, Model Numbers and Catalog Numbers ROL B FOR VLT400SF STP - ARDROL309001A, ROL B FOR VLT400SF ...](https://isitonrecall.com/recall/fda-device-z-0758-2024-maquet-volista-volista-access-volista-access-ii-volista-standop-or-light-system-model-numbers-and-ca/) A potential for a light system to fall in the operating room. Class II Reported ongoing Distribution: US Nationwide. Global Distribution. [Official source for Maquet Volista, Volista Access, Volista Access II, Volista Standop OR Light System, Model Numbers...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0758-2024%22) ## Reasons in these listed records - Sevoflurane used with the vaporizer may degrade to hydrogen fluoride, which could present a risk to patients or health care providers through inhalation and/or skin exposure. Potential harms include irritation of respiratory tract, which in worst case may lead to lung edema an... - Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay - The recall is prompted by a defective charger unit (0970.2873) for models 1133.22B4, 1133.22B5, and 1133.22F5 of the ALPHAMAXX mobile operating table. This issue poses a risk of inadequate charging and operational failure. - Potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any of which could lead to a hazardous situation. These examples come from this result page and are not a ranking of every recall reason. ## Checking Getinge Usa Sales Inc ### Is there a recall on getinge usa sales inc right now? This archive contains 48 records, including 46 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 Getinge Usa Sales Inc](https://isitonrecall.com/check/?q=Getinge%20Usa%20Sales%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)