Hazard

Stroke recalls

12 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total: 12
Critical: 0
Severe: 12
Most recent: 2025-03-19

Of the 12 stroke recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 12 (100%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all stroke recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1–12 of 12

SevereFDA (Devices)·Z-1306-2025·2025-03-19
Aortic Root Cannula Recall for Loose Male Luer Component
Medtronic is recalling 316,205 aortic root cannulas due to unexpected loose material in the male luer connector. If not identified before use, this defect could cause stroke; if identified, it may delay surgery.
Product
Aortic Root Cannula: 1. DLP Aortic Root Cannula A. CANNULA 11012 AR FLOWGUARD 12GA, model no 11012 B. CANNULA 11014 AR FLOWGUARD 14GA, model no. 11014 2. MiAR Cannula: A. CANNULA 11012L AR FLOWGUARD LONG 12GA, model no 11012L B. CANNULA 11014L AR FLOWGUARD 14FR LONG, m
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1486-2023·2023-05-17
Emboli Capture Guidewire System Recalled Due to Potential Component Separation
Cordis US Corp recalls 54 units of the ANGIOGUARD RX/XP Emboli Capture Guidewire System due to potential separation of device components. This could delay procedures or result in unplanned intervention, including possible stroke.
Product
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RMC
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1483-2023·2023-05-17
ANGIOGUARD RX / XP Emboli Capture Guidewire System separation during procedures
The ANGIOGUARD RX / XP emboli capture guidewire system may separate from its delivery sheath during medical procedures, potentially leading to stroke or complications requiring emergency intervention.
Product
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RMC
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1493-2023·2023-05-17
ANGIOGUARD Emboli Capture Guidewire System recalled due to potential device separation
Cordis US Corp's ANGIOGUARD RX/XP Emboli Capture Guidewire System is being recalled by the FDA (Class I) because the delivery system and capture sheath may separate during medical procedures, potentially requiring emergency intervention.
Product
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RE
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1495-2023·2023-05-17
Emboli Capture Guidewire System Separation Risk Recalls ANGIOGUARD RX/XP
Cordis US Corp is recalling ANGIOGUARD RX/XP Emboli Capture Guidewire Systems worldwide due to potential separation of the delivery system and capture sheath during procedures, which could cause stroke or require emergency intervention.
Product
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RM
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1485-2023·2023-05-17
ANGIOGUARD RX/XP Guidewire System May Separate During Medical Procedures
The ANGIOGUARD RX/XP Emboli Capture Guidewire System may separate during medical procedures, potentially delaying treatment or requiring unplanned intervention. The recall affects 471 units distributed worldwide.
Product
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RMC
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1491-2023·2023-05-17
Emboli Capture Guidewire System recalled due to potential device separation
Cordis US Corp is recalling the ANGIOGUARD RX/XP Emboli Capture Guidewire System (1,087 units worldwide) due to potential separation of the delivery system and capture sheath, which could lead to stroke.
Product
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RE
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1490-2023·2023-05-17
ANGIOGUARD RX/XP Emboli Capture Guidewire System May Separate During Procedures
ANGIOGUARD RX/XP emboli capture guidewire systems may separate from their delivery sheaths during interventional procedures, potentially causing stroke. Cordis is recalling 56 units distributed worldwide.
Product
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RM
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1487-2023·2023-05-17
Emboli Capture Guidewire System Separation Hazard Prompts FDA Recall
The ANGIOGUARD RX/XP Emboli Capture Guidewire System may separate from its delivery sheath during medical procedures, potentially causing stroke or requiring emergency surgery. Cordis US Corp is recalling 146 units worldwide.
Product
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 801814RMC
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1494-2023·2023-05-17
Emboli Capture Guidewire System recalled for component separation risk
The ANGIOGUARD RX/XP Emboli Capture Guidewire System is being recalled because the delivery system and capture sheath may separate during procedures, potentially causing stroke or requiring emergency surgical intervention.
Product
ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RM
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-2439-2020·2020-07-08
LivaNova SCP Pump Control Panel Recalled for Rotary Knob Wear
LivaNova is recalling eight SCP Pump Control Panels because premature wear of the angle encoder may make the rotary knob difficult or impossible to rotate during cardiopulmonary bypass.
Product
Control Panel REF - 60-02-50: LivaNova SCP Pump Control Panel S5/C5. REF 60-02-50, IPX2, RxOnly, UDI: 04033817900993
Category
Medical Device
Distribution
13 states
SevereFDA (Devices)·Z-2440-2020·2020-07-08
LivaNova SCP Pump Control Panel Recalled Due to Rotary Knob Wear
LivaNova is recalling 24 SCP Pump Control Panels because the rotary knob may fail to rotate due to premature wear, risking patient injury during surgery.
Product
Control Panel REF - 60-02-15: LivaNova SCP Pump Control Panel. REF 60-02-15, IPX2, RxOnly, UDI: 04033817900986
Category
Medical Device
Distribution
13 states