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Zplp distal lateral fibular plate

Official notice

8 Apr 2024

Last checked

8 Apr 2024

Medium riskHealth Canada
Watch Zimmer

An official Health Canada notice concerns Zplp distal lateral fibular plate. This recall is due to a possible thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock. There are no specific patient monitoring instructions recommended beyond the existing follow-up schedule for previously implanted products. The issue was discovered through a complaint investigation. There have been 24 complaints received. Recall Start Date: March 27, 2024 Published 2024-04-08.

What to do now

Contact the manufacturer if you require additional information.

Recall number

75364

Official notice

2024-04-08

The hazard

This recall is due to a possible thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock. There are no specific patient monitoring instructions recommended beyond the existing follow-up schedule for previously implanted products. The issue was discovered through a complaint investigation. There have been 24 complaints received. Recall Start Date: March 27, 2024

How to check if you're affected

Compare the VIN on your vehicle against the official list. If your VIN is listed, follow the official notice.

Recall Numbers

75364

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Affected products

Product 1

Affected products - ZPLP Distal Lateral Fibular Plate, Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalog number - 00235701706 00235701810 00235701704 00235701710 00235701708 00235701804 00235701806 00235701808

Risk / hazard

This recall is due to a possible thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the screw may not correctly lock. There are no specific patient monitoring instructions recommended beyond the existing follow-up schedule for previously implanted products. The issue was discovered through a complaint investigation. There have been 24 complaints received. Recall Start Date: March 27, 2024

Where it was sold

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

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Brand

Zimmer, Zplp Distal Lateral Fibular Plate

Manufacturer

Not provided

Phone

Not provided

Brand: Zimmer, Zplp Distal Lateral Fibular Plate.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

75364

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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