Recall archive / FDA device enforcement
HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 20mmx10mm UPN: M00553560 — FDA record Z-1036-2025
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Dec 20, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 20mmx10mm UPN: M00553560
- Reason
- Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
- Classification
- Class II
- Recalling firm
- Boston Scientific Corporation
- Quantity
- 1102 units (OUS)
- Agency-reported status
- Ongoing
- Source record identifier
- Z-1036-2025
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | GTIN: 08714729951100 Lot Numbers: 32865866, 32874910, 32875944, 32876867, 32876869, 32876870, 33195387, 33195388, 33195389, 33195390, 33209841, 33209843, 33215357, 33283337, 33284518, 33284519, 33288532, 33288534, 33301346, 33301347, 33301348, 33301351, 33301352, 33466658, 33467021, 33470461, 33470464, 33470465, 33486865, 33487939, 33519203, 33528652, 33581298, 33581681, 33601247, 33657824, 33686163, 33686166, 33765267, 33804643, 33806748, 33909812, 33909813, 33920980, 33948082, 33977789, 33981155, 33981156, 34006718, 34015882, 34020432, 34020433, 34020434, 34027240, 34047363, 34065574, 34074522, 34076577, 34083205, 34085563, 34101925, 34102569, 34102570, 34102571, 34103179, 34103340, 34111453, 34111454, 34111456, 34111845, 34116472, 34116473, 34126522, 34180835, 34190940, 34190949, 34201914, 34205933, 34205934, 34213826, 34214585, 34214586, 34223572, 34223574, 34325972, 34325974, 34334692, 34335366, 34371087, 34371088, 34371090, 34523681, 34545213, 34649321, 34815303 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Nationwide including Puerto Rico Foreign: To be provided
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
Dates in the source
- Report date
- Feb 5, 2025
- Recall initiation date
- Dec 20, 2024
- Center classification date
- Jan 30, 2025
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.