No image published for this recall

No image published for this recall

Depuy Orthopaedics LCS Complete Knee Revision System VVC Insert Product Usage: LCS VVC Insert is used in Knee Revision Surgery - safety alert

Official notice

14 Dec 2016

Last checked

14 Dec 2016

Medium riskFDA

An official FDA notice concerns Depuy Orthopaedics LCS Complete Knee Revision System VVC Insert Product Usage: LCS VVC Insert is used in Knee Revision Surgery - safety alert. An official FDA notice concerns LCS Complete Knee Revision System VVC Insert Product Usage: LCS VVC Insert is used in Knee Revision Surgery. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2016-12-14. Lots: C08294. Recall numbers: Z-0703-2017. Check the official notice for the complete list. Published 2016-12-14.

What to do now

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

Units affected

1

Recall number

Z-0703-2017

Official notice

2016-12-14

The hazard

An official FDA notice concerns LCS Complete Knee Revision System VVC Insert Product Usage: LCS VVC Insert is used in Knee Revision Surgery. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2016-12-14. Lots: C08294. Recall numbers: Z-0703-2017. 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

C08294

Event Ids

75608

Recall Numbers

Z-0703-2017

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Affected products

Product 1

LCS Complete Knee Revision System VVC Insert Product Usage: LCS VVC Insert is used in Knee Revision Surgery

Units affected

1

Risk / hazard

An official FDA notice concerns LCS Complete Knee Revision System VVC Insert Product Usage: LCS VVC Insert is used in Knee Revision Surgery. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2016-12-14. Lots: C08294. Recall numbers: Z-0703-2017. 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: Depuy Orthopaedics. Contact: DePuy Orthopaedics, Inc..

Source & status

Source

Tier

official

Category

ELECTRONICS

App estimate

medium

Recall details

Recall number

Z-0703-2017

Event id

75608

Units affected

1

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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