Use caution Medical device recall · FDA · Published December 17, 2018

Stryker BW Lasso 2515 ANV eco Variable EP Catheters: EEPROM Error Risk with CARTO Systems

Stryker recalls BW Lasso 2515 ANV eco Variable Diagnostic EP Catheters with specific lot codes due to potential EEPROM chip errors when used with CARTO EP Navigation Systems.

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

🇺🇸 FDA recall #Z-0766-2019Medical device Stryker Sustainability Solutions ›

Use caution until it’s fixed

Stryker s Sustainability Solutions division (SSS) has received an increase in reports indicating that an EEPROM chip error code may occur when Reprocessed 2515 NAV eco Variable Electrophysiology (EP) Catheters are used with CARTO(R) EP Navigation Systems.

Take action

Contact the company

Recalling firmStryker Sustainability Solutions1810 W Drake Dr · Tempe, AZ 85283-4327

✎ GovInfoNow plain-language explainer

Stryker is recalling certain BW Lasso 2515 ANV eco Variable Diagnostic EP Catheters because an EEPROM chip error may occur when reprocessed catheters are used with CARTO EP Navigation Systems. This could lead to incorrect diagnostic readings during medical procedures. Read more at govinfonow.com/recall/69328-stryker-bw-lasso-2515-anv-eco-variable-ep-catheters-eeprom.

Source Summary by GovInfoNow · govinfonow.com/recall/69328-stryker-bw-lasso-2515-anv-eco-variable-ep-catheters-eeprom · Updated August 20, 2026 · FDA enforcement record: FDA #Z-0766-2019

Cite this page

“Stryker BW Lasso 2515 ANV eco Variable EP Catheters: EEPROM Error Risk with CARTO Systems.” GovInfoNow, updated August 20, 2026. https://govinfonow.com/recall/69328-stryker-bw-lasso-2515-anv-eco-variable-ep-catheters-eeprom. Based on FDA recall #Z-0766-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0766-2019%22&limit=1).

The FDA announced on Dec. 17, 2018, that Stryker Sustainability Solutions is recalling BW Lasso 2515 ANV eco Variable Diagnostic EP Catheters due to potential EEPROM chip error codes. The recall affects 103 units distributed in the U.S. and internationally.

How to tell if you have it

Brand: Stryker Sustainability Solutions
Product: BW Lasso 2515 ANV eco Variable Diagnostic EP Catheter, REF D134301
Lot Codes: 2674940, 2724318, 2761521, 2794036, 2879309, 2918829, 2677298, 2724320, 2763683, 2794073, 2879312, 2920167, 2677324, 2726887, 2767521, 2794191, 2887266, 2925629, 2677325, 2727015, 2767528, 2804281, 2887691, 2925630, 2677326, 2727016, 2767537, 2843017, 2889131, 2925632, 2677327, 2732728, 2777174, 2843547, 2892701, 2925633, 2677328, 2736609, 2777175, 2862775, 2893277, 2930750, 2677331, 2742516, 2777185, 2862776, 2896226, 2930753, 2677398, 2742579, 2777186, 2869100, 2896229, 2941324, 2677399, 2742580, 2777187, 2871151, 2898832, 2970121, 2683282, 2746664, 2786407, 2873812, 2898836, 2970300, 2692529, 2746673, 2786426, 2873898, 2898840, 2970301, 2692536, 2751680, 2786502, 2873899, 2898845, 2970302, 2719705, 2755589, 2786506, 2873924, 2898846, 2986705, 2719707, 2755641, 2786537, 2873935, 2906003, 2993057, 2724210, 2755694, 2786538, 2875420, 2906077, 3002383, 2724283, 2761520, 2786568, 2876114, 2917968, 3002384, 3007144

The hazard

The FDA said the hazard involves an increase in reports indicating that an EEPROM chip error code may occur when Reprocessed 2515 NAV eco Variable Electrophysiology (EP) Catheters are used with CARTO(R) EP Navigation Systems.

Context

GovInfoNow's records show Stryker Sustainability Solutions has 22 other recalls on record since Dec. 1, 2017. Other recent recalls of similar products include Stryker XCEL Bladeless Trocar W/Optiview (Aug. 19, 2026), Bard EP XT Decapolar Catheter (Aug. 18, 2026), and Stryker Daig Livewire Steerable BDB Catheter (April 10, 2026). Other recent recalls of similar products include Codman CerebroFlo EVD Catheter (April 10, 2026) and American Contract Systems Convenience Kit Recall (June 29, 2026).

How to tell if you have this one

Check the lot codes listed in the recall notice: 2674940, 2724318, 2761521, 2794036, 2879309, 2918829, 2677298, 2724320, 2763683, 2794073, 2879312, 2920167, 2677324, 2726887, 2767521, 2794191, 2887266, 2925629, 2677325, 2727015, 2767528, 2804281, 2887691, 2925630, 2677326, 2727016, 2767537, 2843017, 2889131, 2925632, 2677327, 2732728, 2777174, 2843547, 2892701, 2925633, 2677328, 2736609, 2777175, 2862775, 2893277, 2930750, 2677331, 2742516, 2777185, 2862776, 2896226, 2930753, 2677398, 2742579, 2777186, 2869100, 2896229, 2941324, 2677399, 2742580, 2777187, 2871151, 2898832, 2970121, 2683282, 2746664, 2786407, 2873812, 2898836, 2970300, 2692529, 2746673, 2786426, 2873898, 2898840, 2970301, 2692536, 2751680, 2786502, 2873899, 2898845, 2970302, 2719705, 2755589, 2786506, 2873924, 2898846, 2986705, 2719707, 2755641, 2786537, 2873935, 2906003, 2993057, 2724210, 2755694, 2786538, 2875420, 2906077, 3002383, 2724283, 2761520, 2786568, 2876114, 2917968, 3002384, 3007144.

Brand
Stryker Sustainability Solutions
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Lot Codes
Verify the lot code on your catheter against the list of affected lot codes provided in the recall notice.

Where it went and when

Where it was distributed

Distributed in 7 states, and outside the U.S.

FDA distribution: “US distribution to states of: GA, KS, MO FL, CA, WA, IA,; and internationally to: Germany, Japan and Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California, Florida, Georgia, Iowa, Kansas, Missouri, Washington.

Recall timeline

FDA terminated this recall 5 years after the firm started it.

Dec 17, 2018Firm started the recall
Jan 23, 2019FDA classified it Class II
Jan 30, 2019Published in FDA’s Enforcement Report
Dec 8, 2023FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/69328-stryker-bw-lasso-2515-anv-eco-variable-ep-catheters-eeprom">Stryker BW Lasso 2515 ANV eco Variable EP Catheters: EEPROM Error Risk with CARTO Systems (GovInfoNow)</a>

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-0766-2019 (December 17, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0766-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 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.