Recall Monitor
Health Products

ViziShot 2 Flex

· Published by Health Canada · Official notice

Details

Alert type: Health product recall
Category: Health products - Medical devices - General and plastic surgery
Product: ViziShot 2 Flex
Issue: Medical devices - Labelling and packaging, Medical devices - Performance
What to do: Contact the manufacturer if you require additional information.
Audience: Healthcare
Recall class: Type II
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Products

Affected productsLot or serial numberModel or catalogue number
ViziShot 2 FlexMore than 10 numbers, contact manufacturer.NA-U403SX-4019

Issue

Olympus is removing all unexpired ViziShot 2 Flex (19g) devices due to a potential patient safety issue. Customers should not use any of the affected devices listed in the medical device recall letter and should return any affected products. Olympus is also reinforcing existing warnings in the Instructions for Use (IFU).

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