FDA Device recall Z-2273-2025
Carotid WALLSTENT Monorail Endoprosthesis Closed Cell Self-Expanding Stent, stent and stent delivery system
- FDA Device
- Class I
- ongoing
- Published 2025-08-20
On 2025-08-20 the FDA classified a Class I recall of Carotid WALLSTENT Monorail Endoprosthesis Closed Cell Self-Expanding Stent, stent and stent delivery system by Boston Scientific, citing certain batches are being removed due to an increase in complaints received in which physicians encountered greater than anticipated resistance while attempting to withdraw the st….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2273-2025 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2025-07-07 |
| Published | 2025-08-20 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Boston Scientific |
| Distribution | US |
Product
Carotid WALLSTENT Monorail Endoprosthesis Closed Cell Self-Expanding Stent, stent and stent delivery system. Material numbers: H7493915010240 CAROTID WALLSTENT MONORAIL 10.0-24; H7493915010310 CAROTID WALLSTENT MONORAIL 10.0-31; H749391506220 CAROTID WALLSTENT MONORAIL 6.0-22; H749391508210 CAROTID WALLSTENT MONORAIL 8.0-21; H749391508290 CAROTID WALLSTENT MONORAIL 8.0-29; H965SCH647010 CAROTID WALLSTENT MONORAIL 6.0-22; H965SCH647070 CAROTID WALLSTENT MONORAIL 8.0-21; H965SCH647080 CAROTID WALLSTENT MONORAIL 8.0-29; H965SCH647090 CAROTID WALLSTENT MONORAIL 8.0-36; H965SCH647120 CAROTID WALLSTENT MONORAIL 10.0-24; H965SCH647130 CAROTID WALLSTENT MONORAIL 10.0-31; H965SCH647140 CAROTID WALLSTENT MONORAIL 10.0-37; M001719000 CAROTID WALLSTENT MR 6X22 5F 135CM; M001719010 CAROTID WALLSTENT MR 8X21 5F 135CM; M001719020 CAROTID WALLSTENT MR 8X29 5F 135CM; M001719030 CAROTID WALLSTENT MR 8X36 5F 135CM; M001719040 CAROTID WALLSTENT MR 10X24 5.9F 135CM; M001719050 CAROTID WALLSTENT MR 10X31 5.9F 135CM; M001719060 CAROTID WALLSTENT MR 10X37 5.9F 135CM;
Reason
Certain batches are being removed due to an increase in complaints received in which physicians encountered greater than anticipated resistance while attempting to withdraw the stent delivery system (SDS) from the guidewire or embolic protection device (EPD) after successful stent deployment. The most serious potential adverse health consequence is stroke. Other risks include delay to procedure, vessel injury, vessel spasm, or stent disruption/damage necessitating additional intervention.
Identifiers
| code_info | 1. H7493915010240 UDI-DI 08714729781097 Batches 35277608 35315983 35315984 35315985 35380314 35452835 35452836 35514614…1. H7493915010240 UDI-DI 08714729781097 Batches 35277608 35315983 35315984 35315985 35380314 35452835 35452836 35514614 35551688 35551689 35664523 35664524 35750157 35750158 35750159 35750400 35879409 35879410 35921915 35922951 35926817 35926818 35942366 36056965 36058841 36058842 36058843 36096638 36121883 36138618 36138619 36138801 36138802 36138803 36159671 36195057 36195058 36195059 36195360 36205167 36209423 36214805 36214806 36256192 36322725 36348207 36348208 36348209 36498256 36588496 36607566 36711321; 2. H7493915010310 UDI-DI 08714729781110 Batches 35294379 35294540 35295922 35330503 35330504 35336132 35347263 35382292 35383351 35383352 35453002 35461487 35461488 35528579 35529200 35628964 35628965 35628966 35641995 35662047 35664484 35664485 35750401 35750402 35750403 35750404 35750405 35750406 35750407 35890012 35893584 35893585 35894358 35894359 35938922 35938923 35938924 35938925 35938926 36002641 36002642 36063291 36063292 36105446 36133161 36134808 36144148 36148535 3 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2273-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.