--- title: "Argon Medical Devices, Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Argon Medical Devices, 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/argon-medical-devices-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Argon Medical Devices, Inc recall records **14** reported ongoing 14 records in this archive. Latest source date Jun 15, 2026. 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 Jun 15, 2026 FDA device enforcement ### [L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 18ga (3.5F) 1.15mm x 60cm, REF: 384464; Basic Kit 28GA (1.2F) x 25cm 1 Lumen), RE...](https://isitonrecall.com/recall/fda-device-z-2803-2026-l-cath-picc-s-l-peripherally-inserted-central-catheter-26ga-1-9f-0-60mm-x-30cm-ref-384539-18ga-3-5f/) Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking and/or cracking at the hub, which may lead to replacement, inability to flush/... Class II Reported ongoing Distribution: US: AR, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, MA, MD, MI, MN, MO, MS, NC, ND, NJ, NV, NY, OR, TN, TX, UT, VA, WA. OUS: MYS, CAN, SAU [Official source for L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 1...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2803-2026%22) Jun 15, 2026 FDA device enforcement ### [L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620](https://isitonrecall.com/recall/fda-device-z-2804-2026-l-cath-midline-s-l-catheter-20ga-3f-1mm-x-20cm-ref-384620/) Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking and/or cracking at the hub, which may lead to replacement, inability to flush/... Class II Reported ongoing Distribution: US: AR, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, MA, MD, MI, MN, MO, MS, NC, ND, NJ, NV, NY, OR, TN, TX, UT, VA, WA. OUS: MYS, CAN, SAU [Official source for L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2804-2026%22) Jun 1, 2026 FDA device enforcement ### [Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F, REF: 008416A, 008566A](https://isitonrecall.com/recall/fda-device-z-2704-2026-transvenous-pacing-electrode-tray-w-bipolar-balloon-pacing-electrode-5f-ref-008416a-008566a/) Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. Class I Reported ongoing Distribution: Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago. [Official source for Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing Electrode 5F, REF: 008416A, 008566A](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2704-2026%22) Jun 1, 2026 FDA device enforcement ### [One-Piece Introducer Tray, REF: 497455, 497434 cardiovascular](https://isitonrecall.com/recall/fda-device-z-2705-2026-one-piece-introducer-tray-ref-497455-497434-cardiovascular/) Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. Class I Reported ongoing Distribution: Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago. [Official source for One-Piece Introducer Tray, REF: 497455, 497434 cardiovascular](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2705-2026%22) Jun 1, 2026 FDA device enforcement ### [General Biospy Tray, REF: GUTS1000](https://isitonrecall.com/recall/fda-device-z-2706-2026-general-biospy-tray-ref-guts1000/) Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. Class I Reported ongoing Distribution: Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago. [Official source for General Biospy Tray, REF: GUTS1000](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2706-2026%22) Jun 1, 2026 FDA device enforcement ### [T-Lok Bone Marrow Tray, REF: BMT1104STL; BMET1104TL; BMT1104CATL](https://isitonrecall.com/recall/fda-device-z-2707-2026-t-lok-bone-marrow-tray-ref-bmt1104stl-bmet1104tl-bmt1104catl/) Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. Class I Reported ongoing Distribution: Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago. [Official source for T-Lok Bone Marrow Tray, REF: BMT1104STL; BMET1104TL; BMT1104CATL](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2707-2026%22) Jun 1, 2026 FDA device enforcement ### [Arterial Line Kit 20ga x 6, REF: 400115A](https://isitonrecall.com/recall/fda-device-z-2708-2026-arterial-line-kit-20ga-x-6-ref-400115a/) Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. Class I Reported ongoing Distribution: Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago. [Official source for Arterial Line Kit 20ga x 6, REF: 400115A](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2708-2026%22) Jun 1, 2026 FDA device enforcement ### [Bone Marrow Tray, REF: CB0033TL; CB0355TLA](https://isitonrecall.com/recall/fda-device-z-2709-2026-bone-marrow-tray-ref-cb0033tl-cb0355tla/) Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. Class I Reported ongoing Distribution: Distribution US nationwide including Puerto Rico; OUS to Trinidad and Tobago. [Official source for Bone Marrow Tray, REF: CB0033TL; CB0355TLA](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2709-2026%22) Sep 12, 2025 FDA device enforcement ### [Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated for the prevention of recurrent pulmonary embolism (PE) via ...](https://isitonrecall.com/recall/fda-device-z-0589-2026-option-elite-vena-cava-filter-system-ref-352506070e-udi-di-code-00886333217151-the-option-elite-filt/) Due to complaints of increased resistance when advancing the dilator within the introducer sheath. This issue could potential result in procedural delays and/or risk of venous intimal injuries if excessive force is applied Class II Reported ongoing Distribution: U.S. (nationwide) distribution to states of: AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NM, NV, NY, OH, ... [Official source for Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0589-2026%22) Jul 2, 2024 FDA device enforcement ### [BioPince Ultra Full Core Biopsy Instrument: REF: REF: 360-1080-01, 360-1080-02, 360-1080-03, 360-1580-01, 360-1580-02, 360-1580-03, 360-2080-01, 360-2080-02, 360-2080-03, 370-10...](https://isitonrecall.com/recall/fda-device-z-3192-2024-biopince-ultra-full-core-biopsy-instrument-ref-ref-360-1080-01-360-1080-02-360-1080-03-360-1580-01-3/) Holes have been identified in biopsy instrument packaging trays compromising the sterile barrier, which may lead to cross contamination, or the introduction of micro-organisms into the access site, which could lead to an infectious process, bacteremia, or s... Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution including in the states of AZ, FL, OH, NY, MO, CO, IL, NC, CA, AK, PA, MN, ND, TX, SC, AR, WI, OK, TN, KS, UT, NJ, VA, MA, KY, IN, AL, DE,... [Official source for BioPince Ultra Full Core Biopsy Instrument: REF: REF: 360-1080-01, 360-1080-02, 360-1080-03, 360-...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3192-2024%22) Jun 14, 2024 FDA device enforcement ### [L-CATH PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) 0.60mm x 30cm, REF: 384539](https://isitonrecall.com/recall/fda-device-z-2638-2024-l-cath-picc-s-l-peripherally-inserted-central-catheter-26ga-1-9f-0-60mm-x-30cm-ref-384539/) Peripherally Inserted Central Catheter (PICC) is labeled 26G/1.9Fr x 30cm but package contains incorrect 26G/1.9Fr x 50cm PICC, which could lead to procedural delay. Class II Reported ongoing Distribution: US distribution to the states of: TX, WA, CA, IL [Official source for L-CATH PICC S/L Peripherally Inserted Central Catheter, 26Ga (1.9F) 0.60mm x 30cm, REF: 384539](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2638-2024%22) Jun 8, 2023 FDA device enforcement ### [Argon Medical Devices, REF 352506070E, Option Elite Retrievable Vena Cava Filter, Suitable of Jugular or Femoral Delivery, STERILEO, RxOnly, CE 2797](https://isitonrecall.com/recall/fda-device-z-2239-2023-argon-medical-devices-ref-352506070e-option-elite-retrievable-vena-cava-filter-suitable-of-jugular-o/) There is the potential that the vena Cava Filter may not perform as intended which may result in pulmonary embolism. Class II Reported ongoing Distribution: US Nationwide distribution in the state of TX. [Official source for Argon Medical Devices, REF 352506070E, Option Elite Retrievable Vena Cava Filter, Suitable of Jug...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2239-2023%22) Jan 24, 2022 FDA device enforcement ### [1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6"](https://isitonrecall.com/recall/fda-device-z-0563-2022-1-arterial-line-kit-20ga-x-6-2-arterial-line-kit-1-20ga-x-6/) Guidewire included with two lots of Arterial Line Kits would not fit through the needle of the same kit. This could potentially lead to a slight delay in the procedure and minor blood loss. Class II Reported ongoing Distribution: US Nationwide distribution in the states of AL, CA, DE, IL, IN, LA, MT, NV, OH, TX, VA, TN. [Official source for 1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6"](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0563-2022%22) Oct 4, 2021 FDA device enforcement ### [SuperCore Biopsy Instrument: REF/Product Description: 701114090/SUPERCORE BIOPSY INSTR 14GA X 9CM; 701114150/SUPERCORE BIOPSY INSTR 14GA X 15CM; 701116090/SUPERCORE BIOPSY INSTR...](https://isitonrecall.com/recall/fda-device-z-0354-2022-supercore-biopsy-instrument-ref-product-description-701114090-supercore-biopsy-instr-14ga-x-9cm-7011/) Due to component (housing and plunger) detaching from the semi-automatic biopsy instruments. Class II Reported ongoing Distribution: Worldwide distribution - U.S. Nationwide distribution in the states of AK, AL, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NH, NJ... [Official source for SuperCore Biopsy Instrument: REF/Product Description: 701114090/SUPERCORE BIOPSY INSTR 14GA X 9CM...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0354-2022%22) ## Reasons in these listed records - Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking and/or cracking at the hub, which may lead to replacement, inability to flush/aspirate catheter, c... - Kits containing Lidocaine HCL Injection USP 1% 10mg/mL 5mL ampules subject to another recall recalled due to not meeting release criteria for sterility. - Due to complaints of increased resistance when advancing the dilator within the introducer sheath. This issue could potential result in procedural delays and/or risk of venous intimal injuries if excessive force is applied - Holes have been identified in biopsy instrument packaging trays compromising the sterile barrier, which may lead to cross contamination, or the introduction of micro-organisms into the access site, which could lead to an infectious process, bacteremia, or sepsis. These examples come from this result page and are not a ranking of every recall reason. ## Checking Argon Medical Devices, Inc ### Is there a recall on argon medical devices, inc right now? This archive contains 14 records, including 14 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 Argon Medical Devices, Inc](https://isitonrecall.com/check/?q=Argon%20Medical%20Devices%2C%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)