--- title: "Percussionaire Corporation Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Percussionaire 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/percussionaire-corporation/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Percussionaire Corporation recall records **7** reported ongoing 7 records in this archive. Latest source date Sep 17, 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 Sep 17, 2025 FDA device enforcement ### [Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) REF: P5-TEE-20 (pack of 20)/ P5-TEE (individual) with In-Line Valve Sentec Instructions for Use](https://isitonrecall.com/recall/fda-device-z-0031-2026-phasitron-5-ipv-in-line-valve-intrapulmonary-percussive-ventilation-ref-p5-tee-20-pack-of-20-p5-tee/) IFU update; in-line valve, with pressure relief seal may leak when used with ventilator; don't use in neonates/infants, with target tidal volumes less-than50mL or less-than10kg- at high risk of cardiopulmonary/neurological compromise due to unrecognized hyp... Class I Reported ongoing Distribution: Worldwide distribution. US nationwide, Russia, Japan, Switzerland, Canada, Qatar, Chile, South Africa, United Kingdom, Israel, Turkey, and UAE [Official source for Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) REF: P5-TEE-20 (pack of 2...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0031-2026%22) Dec 23, 2024 FDA device enforcement ### [VDR4 Phasitron Breathing Circuit Models that contain the venturi component: -A50094 D 5PK, Phasitron Kit, VDR, Single Patient, 5pk -A51001, VDR4 Control Unit Tester -PRT 991, VD...](https://isitonrecall.com/recall/fda-device-z-0960-2025-vdr4-phasitron-breathing-circuit-models-that-contain-the-venturi-component-a50094-d-5pk-phasitron-ki/) Due to internal venturi component getting transiently stuck in the forward position within the breathing circuit and may cause a reduction of amplitude and volume of ventilation. Class I Reported ongoing Distribution: Worldwide - U.S. Nationwide distribution in the states of AZ, FL, IL, MS, MO, NE, NJ, NY, NC, RI, TX, UT, and WV. The countries of Belgium, Canada, France, Hong Kong, Netherland... [Official source for VDR4 Phasitron Breathing Circuit Models that contain the venturi component: -A50094 D 5PK, Phasit...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0960-2025%22) Sep 16, 2024 FDA device enforcement ### [Phasitron5 Breathing Circuit (P5-10, P5-HC, P5-UC-10). component of Intrapulmonary Percussive Ventilation, used to provide airway clearance therapy](https://isitonrecall.com/recall/fda-device-z-0208-2025-phasitron5-breathing-circuit-p5-10-p5-hc-p5-uc-10-component-of-intrapulmonary-percussive-ventilation/) As a result of product complaints, breathing circuits are experiencing discolored fluid which are formed when therapy was being given with specific medication through the nebulizer cup. Discoloration is caused by a reaction between medicated mist and an ina... Class I Reported ongoing Distribution: U.S.: PA, AR, MI, CA, TX, OH, NY, FL, IL, NE, OR, GA, WI, MO, OK, AL, WV, MT, CO, LA, VA, CT, SC, NH, NV, NC, NJ, MI, UT, ID, ME, MN, SD, ID, ND, KS, KY, TN, MD, VT, MA, RI, O.U... [Official source for Phasitron5 Breathing Circuit (P5-10, P5-HC, P5-UC-10). component of Intrapulmonary Percussive Ven...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0208-2025%22) Aug 21, 2024 FDA device enforcement ### [Percussionaire, Inc., REF: P5-TEE, Qty: 1, Rx Only. IPV (Intrapulmonary Percussive Ventilation) therapy In-Line Valve](https://isitonrecall.com/recall/fda-device-z-3207-2024-percussionaire-inc-ref-p5-tee-qty-1-rx-only-ipv-intrapulmonary-percussive-ventilation-therapy-in-lin/) Updated labeling to ensure that blue cap on in-line valve is removed, prior to delivery of (Intrapulmonary percussive ventilation) IPV therapy. Class I Reported ongoing Distribution: US: Nationwide OUS: Israel Japan Russia Switzerland Canada Turkey [Official source for Percussionaire, Inc., REF: P5-TEE, Qty: 1, Rx Only. IPV (Intrapulmonary Percussive Ventilation) t...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3207-2024%22) Aug 21, 2024 FDA device enforcement ### [Percussionaire, Inc., REF: P5-TEE-20, Qty: 20, Rx Only. IPV (Intrapulmonary Percussive Ventilation) therapy In-Line Valve](https://isitonrecall.com/recall/fda-device-z-3208-2024-percussionaire-inc-ref-p5-tee-20-qty-20-rx-only-ipv-intrapulmonary-percussive-ventilation-therapy-in/) Updated labeling to ensure that blue cap on in-line valve is removed, prior to delivery of (Intrapulmonary percussive ventilation) IPV therapy. Class I Reported ongoing Distribution: US: Nationwide OUS: Israel Japan Russia Switzerland Canada Turkey [Official source for Percussionaire, Inc., REF: P5-TEE-20, Qty: 20, Rx Only. IPV (Intrapulmonary Percussive Ventilatio...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3208-2024%22) Dec 12, 2023 FDA device enforcement ### [High Frequency Transport Phasitron Breathing Circuit Kit REF: A50605-D, Rx Only, CE 0123](https://isitonrecall.com/recall/fda-device-z-0637-2024-high-frequency-transport-phasitron-breathing-circuit-kit-ref-a50605-d-rx-only-ce-0123/) Due to an assembly error within the breathing circuit, their pressure output of the breathing circuit kit can be affected and have severe impact to the end user Class I Reported ongoing Distribution: US:AL AR CA CT FL GA IL IN KS LA MI MN MO NC NJ OH OR TN TX UT VA OUS: None [Official source for High Frequency Transport Phasitron Breathing Circuit Kit REF: A50605-D, Rx Only, CE 0123](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0637-2024%22) Mar 28, 2023 FDA device enforcement ### [Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit)](https://isitonrecall.com/recall/fda-device-z-0693-2024-distal-phasitron-part-s20020-for-use-with-percussionaire-vdr-4-control-driver-or-control-unit/) Breathing circuit reservoir bag may be assembled at the wrong attachment point, which will result in less than optimal therapy. Class I Reported ongoing Distribution: US: RI, CA, TX [Official source for Distal Phasitron, Part: S20020, for use with Percussionaire VDR-4 control driver (or control unit)](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0693-2024%22) ## Reasons in these listed records - IFU update; in-line valve, with pressure relief seal may leak when used with ventilator; don't use in neonates/infants, with target tidal volumes less-than50mL or less-than10kg- at high risk of cardiopulmonary/neurological compromise due to unrecognized hypoventilation, update... - Due to internal venturi component getting transiently stuck in the forward position within the breathing circuit and may cause a reduction of amplitude and volume of ventilation. - As a result of product complaints, breathing circuits are experiencing discolored fluid which are formed when therapy was being given with specific medication through the nebulizer cup. Discoloration is caused by a reaction between medicated mist and an inadvertent/unapproved ... - Updated labeling to ensure that blue cap on in-line valve is removed, prior to delivery of (Intrapulmonary percussive ventilation) IPV therapy. These examples come from this result page and are not a ranking of every recall reason. ## Checking Percussionaire Corporation ### Is there a recall on percussionaire 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 Percussionaire Corporation](https://isitonrecall.com/check/?q=Percussionaire%20Corporation) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)