Official recall record

Ultra Intra-Aortic Balloon Pumps (IABP)

Health Canada — Medical Devices · 2024-05-07 · CanadaType I

Issuing authority: Health Canada — Medical Devices
Published: 2024-05-07
Country of alert: Canada
Alert level: Type I
Alert type: recall

What the authority reported

Teleflex is initiating this voluntary correction for the above-mentioned products due to reports indicating an infrequent condition that, when not identified and corrected promptly, could result in serious health consequences. The issue may manifest as: failure of the intra-aortic balloon to completely inflate over its full length damaged or broken central lumen in the segment contained within the balloon helium loss or blood in the helium pathway Recall start date: April 30, 2024

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 — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

More recalls: Health Canada — Medical Devices · Canada · all filters

ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.