# FDA recall Z-2672-2026

> **W L Gore & Associates, Inc.** · Class II · device recall initiated 2026-05-19.

## Product

GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component  Catalog Numbers (by Region)  United States (includes Puerto Rico) and Canada:  TSB080806A, TSB081006A, TSB081206A,  TSB081506A, TSB081706A, TSB121506A, TSB121706A, TSB122006A  EMEA Countries, Australia, New Zealand:  TSB080806E, TSB081006E, TSB081206E,  TSB081506E, TSB081706E, TSB121506E, TSB121706E, TSB122006E  Japan:  TSB080806J, TSB081006J, TSB081206J,  TSB081506J, TSB081706J, TSB121506J,  TSB121706J, TSB122006J  China and Taiwan:  TSB080806W, TSB081006W, TSB081206W,  TSB081506W, TSB081706W, TSB121506W, TSB121706W, TSB122006W    The GORE¿ TAG¿ Thoracic Branch Endoprosthesis is indicated for endovascular repair of lesions of the aortic arch and descending thoracic aorta, while maintaining flow into a single aortic arch branch vessel  The GORE¿ TAG¿ Thoracic Branch Endoprosthesis is a modular device consisting of the Aortic Component (AC), the Side Branch (SB) Component, and an optional Aortic Extender (AE), and their respective delivery systems. These components may be used together as a stand-alone device or in conjunction with the GORE¿ TAG¿ Conformable Thoracic Endoprosthesis to accommodate the intended treatment site.

## Reason for recall

Due to catheter separation

## Distribution

Worldwide - U.S. Nationwide distribution including in the states and territories of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KY, LA, MA, MD, MI, MN, MO, MT, NC, ND, NE, NJ, NM, NY, OH, OR, PA, PR, SC, SD, TN, TX, UT, VA, WA, and WI. The countries of United Arab Emirates, Australia, Austria, Canada, Switzerland, China, Cyprus, Germany, Denmark, Spain, Finland, France, United Kingdom, Greece, Croatia, Hungary, Ireland, Israel, Italy, Japan, Luxembourg, Monaco, Malta, Netherlands, Norway, New Zealand, Poland, Portugal, Saudi Arabia, Slovakia, Sweden, and Taiwan.

## Key facts

- **Recall number:** Z-2672-2026
- **Recalling firm:** W L Gore & Associates, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-19
- **Report date:** 2026-07-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Flagstaff, AZ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2672-2026

## Citation

> MORVS. FDA recall Z-2672-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-2672-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*