Skip to content
Get alerts
GovInfoNow
Use caution Medical device recall · FDA · Published May 3, 2024

Atrium Medical ADVANTA VXT Vascular Graft Recall: Slider GDS Separation Risk

Atrium Medical recalls ADVANTA VXT vascular grafts with reported Slider GDS Swivel Rod separation. Affected units have specific model codes; contact for remedy.

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

🇺🇸 FDA recall #Z-1989-2024Medical deviceAtrium Medical ›
Take action

Contact the company

Recalling firmAtrium Medical Corporation40 Continental Blvd · Merrimack, NH 03054-4332
✎ GovInfoNow plain-language explainer

Atr: Atrium Medical is recalling specific ADVANTA VXT vascular graft models due to reported separation of the Slider GDS Swivel Rod from the Swivel Core, creating a gap between the two parts. This could lead to complications during medical procedures. Read more at govinfonow.com/recall/55180-atrium-medical-advanta-vxt-vascular-graft-recall-slider-gds-separation.

Source Summary by GovInfoNow · govinfonow.com/recall/55180-atrium-medical-advanta-vxt-vascular-graft-recall-slider-gds-separation · Updated August 18, 2026 · FDA enforcement record: FDA #Z-1989-2024

Cite this page

“Atrium Medical ADVANTA VXT Vascular Graft Recall: Slider GDS Separation Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/55180-atrium-medical-advanta-vxt-vascular-graft-recall-slider-gds-separation. Based on FDA recall #Z-1989-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1989-2024%22&limit=1).

Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core, according to the FDA. The agency announced the voluntary Class II recall on May 3, 2024.

How to tell if you have it

  • Brand: Atrium Medical
  • Product: ADVANTA VXT, 6X80, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
  • Product Code: 22225
  • UDI-DI: 00650862222258

The hazard

The recall cites complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. The record does not report specific incidents or injuries.

Context

GovInfoNow's records show Atrium Medical Corporation has 16 other recalls on record since 2017-11-22. Other recent recalls of similar products include Getinge Thoracic Catheter Recall (2026-08-07), Atrium Medical iCast Stent Recall (2024-09-09), and Atrium Oasis Drain Single W/AC Recall (2023-11-01). Other recent recalls of similar products include Merit Medical Vascular Tray Recall (2025-12-04), Merit Medical Allwell Angioplasty Pack Recall (2025-12-04), and Bolton Medical RelayPro Thoracic Stent-Graft System Recall (2026-04-22).

How to tell if you have this one

Check for the model codes 6X80, 1GDS, FH, STR-TW on the ADVANTA VXT vascular grafts. The product code is 22225 and UDI-DI is 00650862222258.

  • Brand
    Atrium Medical
  • Category
    Medical device
FDA recall event · 68 products

All 68 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 - US Nationwide including Puerto Rico, and the countries of AE, AR, AT, AU, BE, BG, BO, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DZ, EC, EE, EG, ES, FI, FR, GB, GR, HK, ID, IE, IL, IQ, IT, JO, JP, KR, KW, LT, LU, LV, ME, MN, MU, MX, MY, NI, NL, NO, NZ, OM, PA, PE, PH, PK, PL, PT, PY, RO, RU, SA, SE, SG, SI, SV, TH, TN, TR, TW, UA, VN, XK, YE, ZA.
Recall numberProduct, codes & lotsQuantity
Z-1951-2024ADVANTA VXT, 5X40, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft; Product Code: 22011; UDI-DI: 00650862220117.53,308 units (US: 11,236; OUS: 42,072)
Z-1952-2024ADVANTA VXT, 6X40, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft; Product Code: 22012; UDI-DI: 00650862220124.53,308 units (US: 11,236; OUS: 42,072)
Z-1953-2024ADVANTA VXT, 8X40, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft; Product Code: 22014; UDI-DI: 00650862220148.53,308 units (US: 11,236; OUS: 42,072)
Z-1954-2024ADVANTA VXT, 5X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft; Product Code: 22016; UDI-DI: 00650862220162.53,308 units (US: 11,236; OUS: 42,072)
Z-1955-2024ADVANTA VXT, 6X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft; Product Code: 22017; UDI-DI: 00650862220179.53,308 units (US: 11,236; OUS: 42,072)
Z-1956-2024ADVANTA VXT, 7X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft; Product Code: 22018; UDI-DI: 00650862220186.53,308 units (US: 11,236 ; OUS: 42,072)
Z-1957-2024ADVANTA VXT, 8X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft; Product Code: 22019; UDI-DI: 00650862220193.53,308 units (US: 11, 236; OUS: 42,072)
Z-1958-2024ADVANTA VXT, 5X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft; Product Code: 22025; UDI-DI: 00650862220254.53,308 units (US: 11, 236; OUS: 42,072)
Z-1959-2024ADVANTA VXT, 6X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft; Product Code: 22026; UDI-DI: 00650862220261.53,308 units (US: 11, 236; OUS: 42,072)
Z-1960-2024ADVANTA VXT, 7X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft; Product Code: 22027; UDI-DI: 00650862220278.53,308 units (US: 11, 236; OUS: 42,072)
Z-1961-2024ADVANTA VXT, 8X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft; Product Code: 22028; UDI-DI: 00650862220285.53,308 units (US: 11, 236; OUS: 42,072)
Z-1962-2024ADVANTA VXT, 5X40, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft; Product Code: 22058; UDI-DI: 00650862220582.53,308 units (US: 11, 236; OUS: 42,072)
Z-1963-2024ADVANTA VXT, 6X40, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft; Product Code: 22059; UDI-DI: 00650862220599.53,308 units (US: 11, 236; OUS: 42,072)
Z-1964-2024ADVANTA VXT, 5X50, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft; Product Code: 22061; UDI-DI: 00650862220612.53,308 units (US: 11, 236; OUS: 42,072)
Z-1965-2024ADVANTA VXT, 6X50, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft; Product Code: 22062; UDI-DI: 00650862220629.53,308 units (US: 11, 236; OUS: 42,072)
Z-1966-2024ADVANTA VXT, 7X50, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft; Product Code: 22063; UDI-DI: 00650862220636.53,308 units (US: 11, 236; OUS: 42,072)
Z-1967-2024ADVANTA VXT, 8X50, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft; Product Code: 22064; UDI-DI: 00650862220643.53,308 units (US: 11, 236; OUS: 42,072)
Z-1968-2024ADVANTA VXT, 6X70, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft; Product Code: 22070; UDI-DI: 00650862220704.53,308 units (US: 11, 236; OUS: 42,072)
Z-1969-2024ADVANTA VXT, 7X70, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft; Product Code: 22071; UDI-DI: 00650862220711.53,308 units (US: 11, 236; OUS: 42,072)
Z-1970-2024ADVANTA VXT, 8X70, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft; Product Code: 22072; UDI-DI: 00650862220728.53,308 units (US: 11, 236; OUS: 42,072)
Z-1971-2024ADVANTA VXT, 6X80, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft; Product Code: 22075; UDI-DI: 00650862220759.53,308 units (US: 11, 236; OUS: 42,072)
Z-1972-2024ADVANTA VXT, 7X80, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graft; Product Code: 22076; UDI-DI: 00650862220766.53,308 units (US: 11, 236; OUS: 42,072)
Z-1973-2024ADVANTA VXT, 6X40, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22169; UDI-DI: 00650862221695.53,308 units (US: 11, 236; OUS: 42,072)
Z-1974-2024ADVANTA VXT, 8X40, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22170; UDI-DI: 00650862221701.53,308 units (US: 11, 236; OUS: 42,072)
Z-1975-2024ADVANTA VXT, 6X50, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22175; UDI-DI: 00650862221756.53,308 units (US: 11, 236; OUS: 42,072)
Z-1976-2024ADVANTA VXT, 7X50, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22176; UDI-DI: 00650862221763.53,308 units (US: 11, 236; OUS: 42,072)
Z-1977-2024ADVANTA VXT, 6X70, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22185; UDI-DI: 00650862221855.53,308 units (US: 11, 236; OUS: 42,072)
Z-1978-2024ADVANTA VXT, 7X70, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22186; UDI-DI: 00650862221862.53,308 units (US: 11, 236; OUS: 42,072)
Z-1979-2024ADVANTA VXT, 8X70, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22187; UDI-DI: 00650862221879.53,308 units (US: 11, 236; OUS: 42,072)
Z-1980-2024ADVANTA VXT, 6X80, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22190; UDI-DI: 00650862221909.53,308 units (US: 11, 236; OUS: 42,072)
Z-1981-2024ADVANTA VXT, 8X80, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22192; UDI-DI: 00650862221923.53,308 units (US: 11, 236; OUS: 42,072)
Z-1982-2024ADVANTA VXT, 8X40, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22209; UDI-DI: 00650862222098.53,308 units (US: 11, 236; OUS: 42,072)
Z-1983-2024ADVANTA VXT, 6X50, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22212; UDI-DI: 00650862222128.53,308 units (US: 11, 236; OUS: 42,072)
Z-1984-2024ADVANTA VXT, 7X50, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22213; UDI-DI: 00650862222135.53,308 units (US: 11, 236; OUS: 42,072)
Z-1985-2024ADVANTA VXT, 8X50, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22214; UDI-DI: 00650862222142.53,308 units (US: 11, 236; OUS: 42,072)
Z-1986-2024ADVANTA VXT, 6X70, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22220; UDI-DI: 00650862222203.53,308 units (US: 11, 236; OUS: 42,072)
Z-1987-2024ADVANTA VXT, 7X70, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22221; UDI-DI: 00650862222210.53,308 units (US: 11, 236; OUS: 42,072)
Z-1988-2024ADVANTA VXT, 8X70, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22222; UDI-DI: 00650862222227.53,308 units (US: 11, 236; OUS: 42,072)
Z-1989-2024ADVANTA VXT, 6X80, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22225; UDI-DI: 00650862222258.53,308 units (US: 11, 236; OUS: 42,072)
Z-1990-2024ADVANTA VXT, 8X80, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22227; UDI-DI: 00650862222272.53,308 units (US: 11, 236; OUS: 42,072)
Z-1991-2024ADVANTA VXT, 6X100, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22232; UDI-DI: 00650862222326.53,308 units (US: 11, 236; OUS: 42,072)
Z-1992-2024ADVANTA VXT, 6X45, 1GDS, CH, STR-SW. Single-Ended Slider GDS. Vascular graft; Product Code: 22092; UDI-DI: 00650862220926.53,308 units (US: 11, 236; OUS: 42,072)
Z-1993-2024ADVANTA VXT, 4-6X45, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft; Product Code: 22114; UDI-DI: 00650862221145.53,308 units (US: 11, 236; OUS: 42,072)
Z-1994-2024ADVANTA VXT, 4-7X45, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft; Product Code: 22115; UDI-DI: 00650862221152.53,308 units (US: 11, 236; OUS: 42,072)
Z-1995-2024ADVANTA VXT, 5-8X45, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft; Product Code: 22116; UDI-DI: 00650862221169.53,308 units (US: 11, 236; OUS: 42,072)
Z-1996-2024ADVANTA VXT, 4-7X70, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft; Product Code: 22117; UDI-DI: 00650862221176.53,308 units (US: 11, 236; OUS: 42,072)
Z-1997-2024ADVANTA VXT, 4-7X45, 2GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graft; Product Code: 22297; UDI-DI: 00650862222975.53,308 units (US: 11, 236; OUS: 42,072)
Z-1998-2024ADVANTA VXT, 4-6X45, 1GDS, CH, TPR-SW. Single-Ended Slider GDS. Vascular graft; Product Code: 22124; UDI-DI: 00650862221244.53,308 units (US: 11, 236; OUS: 42,072)
Z-1999-2024ADVANTA VXT, 4-7X45, 1GDS, CH, TPR-SW. Single-Ended Slider GDS. Vascular graft; Product Code: 22125; UDI-DI: 00650862221251.53,308 units (US: 11, 236; OUS: 42,072)
Z-2000-2024ADVANTA VXT, 4-7X80, 1GDS, FH, TPR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22266; UDI-DI: 00650862222661.53,308 units (US: 11, 236; OUS: 42,072)
Z-2001-2024ADVANTA VXT, 5-8X80, 1GDS, FH, TPR-TW. Single-Ended Slider GDS. Vascular graft; Product Code: 22267; UDI-DI: 00650862222678.53,308 units (US: 11, 236; OUS: 42,072)
Z-2002-2024FLIXENE, 6X50, 1GDS, GW. Single-Ended Slider GDS. Vascular graft; Product Code: 25058; UDI-DI: 00650862250589.53,308 units (US: 11, 236; OUS: 42,072)
Z-2003-2024FLIXENE, 7X50, 1GDS, GW. Single-Ended Slider GDS. Vascular graft; Product Code: 25059; UDI-DI: 00650862250596.53,308 units (US: 11, 236; OUS: 42,072)
Z-2004-2024FLIXENE, 6X40, 1GDS, GW. Single-Ended Slider GDS. Vascular graft; Product Code: 25061; UDI-DI: 00650862250619.53,308 units (US: 11, 236; OUS: 42,072)
Z-2005-2024FLIXENE, 7X40, 1GDS, GW. Single-Ended Slider GDS. Vascular graft; Product Code: 25062; UDI-DI: 00650862250626.53,308 units (US: 11, 236; OUS: 42,072)
Z-2006-2024FLIXENE, 7X80, 1GDS, GW. Single-Ended Slider GDS. Vascular graft; Product Code: 25120; UDI-DI: 00650862251203.53,308 units (US: 11, 236; OUS: 42,072)
Z-2007-2024FLIXENE, 6X30, 1GDS, GW. Single-Ended Slider GDS. Vascular graft; Product Code: 25125; UDI-DI: 00650862251258.53,308 units (US: 11, 236; OUS: 42,072)
Z-2008-2024FLIXENE, 7X30, 1GDS, GW. Single-Ended Slider GDS. Vascular graft; Product Code: 25126; UDI-DI: 00650862251265.53,308 units (US: 11, 236; OUS: 42,072)
Z-2009-2024FLIXENE, 6X50, 1GDS, STR. Single-Ended Slider GDS. Vascular graft; Product Code: 25052; UDI-DI: 00650862250527.53,308 units (US: 11, 236; OUS: 42,072)
Z-2010-2024FLIXENE, 7X50, 1GDS, STR. Single-Ended Slider GDS. Vascular graft; Product Code: 25056; UDI-DI: 00650862250565.53,308 units (US: 11, 236; OUS: 42,072)
Z-2011-2024FLIXENE, 6X30, 1GDS, STR. Single-Ended Slider GDS. Vascular graft; Product Code: 25142; UDI-DI: 00650862251425.53,308 units (US: 11, 236; OUS: 42,072)
Z-2012-2024FLIXENE, 4-6X35, 2GDS, GWT-GW. Double-Ended Slider GDS. Vascular graft; Product Code: 25128; UDI-DI: 00650862251289.53,308 units (US: 11, 236; OUS: 42,072)
Z-2013-2024FLIXENE, 4-7X35, 2GDS, GWT-GW. Double-Ended Slider GDS. Vascular graft; Product Code: 25129; UDI-DI: 00650862251296.53,308 units (US: 11, 236; OUS: 42,072)
Z-2014-2024FLIXENE, 4-6X45, 2GDS, GWT. Double-Ended Slider GDS. Vascular graft; Product Code: 25134; UDI-DI: 00650862251340.53,308 units (US: 11, 236; OUS: 42,072)
Z-2015-2024FLIXENE, 4-7X45, 2GDS, GWT. Double-Ended Slider GDS. Vascular graft; Product Code: 25135; UDI-DI: 00650862251357.53,308 units (US: 11, 236; OUS: 42,072)
Z-2016-2024FLIXENE, 4-6X45, 2GDS, GWT-GW. Double-Ended Slider GDS. Vascular graft; Product Code: 25137; UDI-DI: 00650862251371.53,308 units (US: 11, 236; OUS: 42,072)
Z-2017-2024FLIXENE, 4-7X45, 2GDS, GWT-GW. Double-Ended Slider GDS. Vascular graft; Product Code: 25138; UDI-DI: 00650862251388.53,308 units (US: 11, 236; OUS: 42,072)
Z-2018-2024FLIXENE, 4-7X30, 2GDS, GWT-GW. Double-Ended Slider GDS. Vascular graft; Product Code: 25141; UDI-DI: 00650862251418.53,308 units (US: 11, 236; OUS: 42,072)
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Verify the model codes 6X80, 1GDS, FH, STR-TW and product code 22225 on the vascular graft.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFLPuerto Rico: yesPR

FDA distribution: “Worldwide distribution - US Nationwide including Puerto Rico, and the countries of AE, AR, AT, AU, BE, BG, BO, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DZ, EC, EE, EG, ES, FI, FR, GB, GR, HK, ID, IE, IL, IQ, IT, JO, JP, KR, KW, LT, LU, LV, ME,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 40 days after the firm started it.

1. Firm started the recall: May 3, 202412. FDA classified it Class II: Jun 4, 202423. Published in FDA’s Enforcement Report: Jun 12, 202432024
  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.

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-1989-2024 (May 3, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1989-2024 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 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