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Cannulated screw system

Official notice

15 Mar 2023

Last checked

15 Mar 2023

Medium riskHealth Canada

An official Health Canada notice concerns Cannulated screw system. The recall is being done because the device does not meet the requirements of the MDR. Specifically, the devices implanted are not on the device system's active license 104252. Recall start date: March 1, 2023 Published 2023-03-15.

What to do now

Contact the manufacturer if you require additional information.

Recall number

73327

Official notice

2023-03-15

The hazard

The recall is being done because the device does not meet the requirements of the MDR. Specifically, the devices implanted are not on the device system's active license 104252. Recall start date: March 1, 2023

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Recall Numbers

73327

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Affected products

Product 1

Affected products - Cannulated Screw System, Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalog number - 00-1402-6066 00-1402-6072 00-1402-6090

Risk / hazard

The recall is being done because the device does not meet the requirements of the MDR. Specifically, the devices implanted are not on the device system's active license 104252. Recall start date: March 1, 2023

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Orthopediatrics, Cannulated Screw System.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

73327

Classification

Type II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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