Brand Recall Hub

Pella Recalls in Canada

18 recalls found for Pella. Data sourced from Health Canada, CFIA, and Transport Canada. Updated daily.

18 Pella Recalls

Medical Devices Type II
2026-08-27

Automated Impella Controller (AIC)

Performance

View recall details →

Medical Devices Type I
2026-06-29

Abiomed Introducer Kits with Impella Heart Pumps

Performance

View recall details →

Medical Devices Type I
2026-05-13

Impella Controller

Performance

View recall details →

Medical Devices Type I
2026-04-28

Automated Impella® Controller

Performance

View recall details →

Medical Devices Type I
2026-03-04

Abiomed Purge Cassette Generation 1 for Impella

Performance

View recall details →

Medical Devices Type I
2026-02-25

Automated Impella Controller

Performance

View recall details →

Medical Devices Type II
2025-10-23

Automated Impella® Controller

Performance

View recall details →

Medical Devices Type I
2025-09-18

Impella Controller

Performance

View recall details →

Medical Devices Type I
2025-08-29

Impella® Controller

Performance

View recall details →

Medical Devices Type I
2025-07-09

Impella® Controller

Performance

View recall details →

Medical Devices Type I
2024-09-05

Impella CP With SmartAssist and Impella 5.5 With SmartAssist

Device compatibility

View recall details →

Medical Devices Type I
2024-03-20

Impella Cp

Device compatibility

View recall details →

Medical Devices Type II
2024-03-12

Impella Products

Labelling and packaging

View recall details →

Medical Devices Type I
2024-03-06

Impella Systems

Labelling and packaging

View recall details →

Consumer Products
2023-12-21

Pella Architect Series Casement Windows Recalled Due to Injury Hazard

Injury hazard

View recall details →

Medical Devices Type II
2023-12-21

Introducer kits in Impella Pump Set and Axillary Insertion Kit

Labelling and packaging

View recall details →

Medical Devices Type II
2022-03-14

Compella

Electrical defect

View recall details →

Medical Devices Type II
2021-01-07

Portex Acapella DH (Green) Vibratory PEP Device with Mouthpiece (2020-12-18)

Medical devices

View recall details →