--- title: "Spectranetics Corporation Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Spectranetics 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/spectranetics-corporation/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Spectranetics Corporation recall records **5** reported ongoing 5 records in this archive. Latest source date Jan 10, 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 10, 2025 FDA device enforcement ### [Intact Vascular Tack Endovascular System, to treat vascular dissections with Tack implant(s) following angioplasty: (4F,1.5-4.5mm), 150cm, REF: 154150041; Tack, 4F Gen 1.5, 150c...](https://isitonrecall.com/recall/fda-device-z-1070-2025-intact-vascular-tack-endovascular-system-to-treat-vascular-dissections-with-tack-implant-s-following/) Use of Tack Endovascular system, designed to treat acute dissections of inner wall or lining of an artery by tacking damaged tissue to inner luminal surface, could result in problems with deployment and stability of device in vessel after deployment, which ... Class I Reported ongoing Distribution: Distribution US nationwide and countries of: NL, DE, NL, AU, IT, CH, GB, and AT [Official source for Intact Vascular Tack Endovascular System, to treat vascular dissections with Tack implant(s) foll...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1070-2025%22) Nov 25, 2024 FDA device enforcement ### [Turbo Elite Laser Atherectomy Catheter Model Number / UDI-DI code / Product Description 414-151 / 989930000531 / 1.4 mm OTW 417-152 / 989930000551 / 1.7 mm OTW 420-006 / 9899300...](https://isitonrecall.com/recall/fda-device-z-0680-2025-turbo-elite-laser-atherectomy-catheter-model-number-udi-di-code-product-description-414-151-98993000/) Due to complaints received for the marker band detaching from the distal tip of the catheter and remaining in the patient as laser catheter was retracted. Class II Reported ongoing Distribution: U.S.: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, ILIN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD TN, TX... [Official source for Turbo Elite Laser Atherectomy Catheter Model Number / UDI-DI code / Product Description 414-151 /...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0680-2025%22) Nov 15, 2023 FDA device enforcement ### [Spectranetics Turbo-Elite Laser Atherectomy Catheter 2.0 RX REF 420-159 Spectranetics Turbo-Elite Laser Atherectomy Catheter 2.0 OTW REF 420-006 Spectranetics Turbo-Elite Laser ...](https://isitonrecall.com/recall/fda-device-z-0509-2024-spectranetics-turbo-elite-laser-atherectomy-catheter-2-0-rx-ref-420-159-spectranetics-turbo-elite-la/) Incorrect product labeling. Exterior product box label does not match internal pouch label. Class II Reported ongoing Distribution: U.S Nationwide - Worldwide Distribution: US Distribution: AL, AR, AZ, CA, CO, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NJ, NV, NY, OH, OK, PA, SC, TN, TX, UT,... [Official source for Spectranetics Turbo-Elite Laser Atherectomy Catheter 2.0 RX REF 420-159 Spectranetics Turbo-Elite...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0509-2024%22) Oct 14, 2022 FDA device enforcement ### [Philips Laser System, REF: LAS-100. Used in minimally invasive interventional procedures within the cardiovascular system, and for the removal of problematic pacemaker and defib...](https://isitonrecall.com/recall/fda-device-z-0221-2023-philips-laser-system-ref-las-100-used-in-minimally-invasive-interventional-procedures-within-the-car/) Laser System may detect Error 106 or Error 108 System Failures that will cause the system to enter non-recoverable safe state. The user will not be able to proceed until the error is cleared. May result in initiation of treatment delay and/or treatment beyo... Class II Reported ongoing Distribution: US: LA, MO, TN, CA, NC, PA, HI, AZ, CO, OK, FL, TX, MN, MI, VA, CT, NY, MD, IL, NJ, MA, KS, ME, AR, IA, IN, GA, ID, OR. OUS: DE, GB, ES, SE, IT, RS, GR, IN, FR, IL, DK, SA [Official source for Philips Laser System, REF: LAS-100. Used in minimally invasive interventional procedures within t...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0221-2023%22) Jun 1, 2022 FDA device enforcement ### [Philips Laser System, REF LAS-100, Intermittent Operation, Duty cycle dependent upon device in use 100 - 240 VAC, 50/60HZ, 16 AM](https://isitonrecall.com/recall/fda-device-z-1351-2022-philips-laser-system-ref-las-100-intermittent-operation-duty-cycle-dependent-upon-device-in-use-100/) The LAS-100 Laser system may detect an inoperable hardware component during power up, which results in an error code and the system not being operable until code is cleared. Class II Reported ongoing Distribution: US: AR AZ CA CO CT FL GA HI IA IL IN KS LA MA MD ME MI MN MO NC NJ NY OK PA TN TX VA OUS: Saudi Arabia, Denmark, France, Greece, India, Italy, Netherlands, Serbia, Spain, Sweden... [Official source for Philips Laser System, REF LAS-100, Intermittent Operation, Duty cycle dependent upon device in us...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1351-2022%22) ## Reasons in these listed records - Use of Tack Endovascular system, designed to treat acute dissections of inner wall or lining of an artery by tacking damaged tissue to inner luminal surface, could result in problems with deployment and stability of device in vessel after deployment, which may cause failure to... - Due to complaints received for the marker band detaching from the distal tip of the catheter and remaining in the patient as laser catheter was retracted. - Incorrect product labeling. Exterior product box label does not match internal pouch label. - Laser System may detect Error 106 or Error 108 System Failures that will cause the system to enter non-recoverable safe state. The user will not be able to proceed until the error is cleared. May result in initiation of treatment delay and/or treatment beyond initial scope and... These examples come from this result page and are not a ranking of every recall reason. ## Checking Spectranetics Corporation ### Is there a recall on spectranetics corporation right now? This archive contains 5 records, including 5 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 Spectranetics Corporation](https://isitonrecall.com/check/?q=Spectranetics%20Corporation) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)