No image published for this recall

No image published for this recall

Zimmer Biomet Vanguard Knee System Series-A Standard Patella sizes 34mm Item Number: 184766 - safety alert

Official notice

6 Mar 2019

Last checked

6 Mar 2019

Medium riskFDA

An official FDA notice concerns Zimmer Biomet Vanguard Knee System Series-A Standard Patella sizes 34mm Item Number: 184766 - safety alert. An official FDA notice concerns Vanguard Knee System Series-A Standard Patella sizes 34mm Item Number: 184766. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2019-03-06. Lots: 381800, 400030. Recall numbers: Z-0938-2019. Check the official notice for the complete list. Published 2019-03-06.

What to do now

The source does not provide specific consumer instructions. Follow the official FDA notice for next steps.

Units affected

90

Recall number

Z-0938-2019

Official notice

2019-03-06

The hazard

An official FDA notice concerns Vanguard Knee System Series-A Standard Patella sizes 34mm Item Number: 184766. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2019-03-06. Lots: 381800, 400030. Recall numbers: Z-0938-2019. Check the official notice for the complete list.

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.

Lots

381800, 400030

Event Ids

82004

Recall Numbers

Z-0938-2019

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Affected products

Product 1

Vanguard Knee System Series-A Standard Patella sizes 34mm Item Number: 184766

Units affected

90

Risk / hazard

An official FDA notice concerns Vanguard Knee System Series-A Standard Patella sizes 34mm Item Number: 184766. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2019-03-06. Lots: 381800, 400030. Recall numbers: Z-0938-2019. Check the official notice for the complete list.

Where it was sold

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

Location 1

US · United States · IN · Warsaw

Affected area 1

US · United States · IN · Warsaw

Affected area 2

US · United States

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Zimmer Biomet. Contact: Zimmer Biomet, Inc..

Source & status

Source

Tier

official

Category

ELECTRONICS

App estimate

medium

Recall details

Recall number

Z-0938-2019

Event id

82004

Units affected

90

Status

terminated

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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