No image published for this recall

No image published for this recall

Biomet Arcos Modular Revision Hip System Standard Cone Prox Body, Size E, 70 MM Item Number:11-301325 - safety alert

Official notice

18 Aug 2021

Last checked

18 Aug 2021

Medium riskFDA

An official FDA notice concerns Biomet Arcos Modular Revision Hip System Standard Cone Prox Body, Size E, 70 MM Item Number:11-301325 - safety alert. An official FDA notice concerns Arcos Modular Revision Hip System Standard Cone Prox Body, Size E, 70 MM Item Number:11-301325. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2021-08-18. Lots: Numbers/UDI. Recall numbers: Z-2269-2021. Check the official notice for the complete list. Published 2021-08-18.

What to do now

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

Units affected

11

Recall number

Z-2269-2021

Official notice

2021-08-18

The hazard

An official FDA notice concerns Arcos Modular Revision Hip System Standard Cone Prox Body, Size E, 70 MM Item Number:11-301325. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2021-08-18. Lots: Numbers/UDI. Recall numbers: Z-2269-2021. 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

Numbers/UDI

Event Ids

88304

Recall Numbers

Z-2269-2021

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Affected products

Product 1

Arcos Modular Revision Hip System Standard Cone Prox Body, Size E, 70 MM Item Number:11-301325

Units affected

11

Risk / hazard

An official FDA notice concerns Arcos Modular Revision Hip System Standard Cone Prox Body, Size E, 70 MM Item Number:11-301325. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2021-08-18. Lots: Numbers/UDI. Recall numbers: Z-2269-2021. 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

Brand

Manufacturer

Not provided

Phone

Not provided

Brand: Biomet. Contact: Biomet, Inc..

Source & status

Source

Tier

official

Category

ELECTRONICS

App estimate

medium

Recall details

Recall number

Z-2269-2021

Event id

88304

Units affected

11

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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