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Official recall record

BVI Safety Knife

Health Canada — Medical Devices · 2024-05-30 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2024-05-30
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

Manufacturer received feedback from a singular customer that the wrong configuration of the blade was in the package. The bevel was on the opposite side, instead of being in front (bevel up) it was in the back (bevel down). There was no injuries or illnesses reported in connection to the associated failure mode. Inadvertently, using a bevel down blade instead of a bevel-up blade causes the surgeon to make an unintended incision architecture. A careful, observant surgeon is likely to notice the incorrect blade orientation under the microscope prior to use. However, when unnoticed, the unintended incision architecture potentially leads to an incision leakage. When incision leakage goes unnoticed , a watertight wound closure may not be achieved and thereby increasing the risk for anterior chamber fluid egress or ocular surface fluid ingress. Health effects include infection, iris prolapse, and intraocular pressure (IOP) fluctuations. Recall start date: May 10, 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.

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