ProductGuru Recalls

Official recall record

Hemospray® Endoscopic Hemostat

Health Canada — Medical Devices · 2024-09-09 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2024-09-09
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

Cook Medical has identified that a limited number of nonconforming raw materials were manufactured into certain lot numbers of hemospray devices and distributed into the field. Use of the devices with these nonconforming raw materials may result in the red activation knob cracking or breaking at the activation knob internal threading while the device is activated. This can lead to the activation knob and carbon dioxide cartridge exiting the handle with force. Recall start date: August 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

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