No image published for this recall

No image published for this recall

Biomet G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462 - safety alert

Official notice

29 Mar 2023

Last checked

29 Mar 2023

Medium riskFDA

An official FDA notice concerns Biomet G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462 - safety alert. An official FDA notice concerns G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2023-03-29. Lots: 65731960. Recall numbers: Z-1284-2023. Check the official notice for the complete list. Published 2023-03-29.

What to do now

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

Units affected

12

Recall number

Z-1284-2023

Official notice

2023-03-29

The hazard

An official FDA notice concerns G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2023-03-29. Lots: 65731960. Recall numbers: Z-1284-2023. 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

65731960

Event Ids

91866

Recall Numbers

Z-1284-2023

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Affected products

Product 1

G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462

Units affected

12

Risk / hazard

An official FDA notice concerns G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2023-03-29. Lots: 65731960. Recall numbers: Z-1284-2023. 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-1284-2023

Event id

91866

Units affected

12

Status

active

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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