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Official recall record

Abiomed Introducer Kits with Impella Heart Pumps

Health Canada · 2026-06-29 · CanadaType I
Issuing authority
Health Canada
Alert date
2026-06-29
Country of alert
Canada
Alert level
Type I
Alert type
recall

What the authority reported

Abiomed has initiated a voluntary medical device recall (correction) for all currently distributed Introducer kits that are used with Impella heart pumps to notify customers of a potential for unexpected introducer sheath leakage from the sidearm and under the sheath cap and along the hub score lines in the hub region. Introducer leakage may impair hemostasis and increase the risk of access-site bleeding, particularly in anticoagulated patients. This information is provided to support appropriate clinical awareness, monitoring, and patient support as needed. The identified defect does not affect any other packaged products within the pump set.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — official record →
Record last checked against the registry on 2026-07-08.

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