No image published for this recall

No image published for this recall

Depuy Orthopaedics GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100 - safety alert

Official notice

19 Jan 2022

Last checked

19 Jan 2022

Medium riskFDA

An official FDA notice concerns Depuy Orthopaedics GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100 - safety alert. An official FDA notice concerns GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2022-01-19. Lots: 9793946. Recall numbers: Z-0490-2022. Check the official notice for the complete list. Published 2022-01-19.

What to do now

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

Units affected

140

Recall number

Z-0490-2022

Official notice

2022-01-19

The hazard

An official FDA notice concerns GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2022-01-19. Lots: 9793946. Recall numbers: Z-0490-2022. 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

9793946

Event Ids

89240

Recall Numbers

Z-0490-2022

Checked manually this time?

The app alerts you when a new official recall is published — no searching, no checking back.

Turn on recall alerts

Affected products

Product 1

GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100

Units affected

140

Risk / hazard

An official FDA notice concerns GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2022-01-19. Lots: 9793946. Recall numbers: Z-0490-2022. 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-0490-2022

Event id

89240

Units affected

140

Status

terminated

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
Something wrong on this page?

Related recalls

US
No image published for this recall

a product listed in the official notice - safety alert

High riskFDA1 Aug 2018
US
No image published for this recall

a product listed in the official notice - safety alert

High riskFDA21 Mar 2018
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA7 Mar 2018
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA27 Jul 2022
US
No image published for this recall

a product listed in the official notice - safety alert

Critical riskFDA13 Jan 2021
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA17 Feb 2016
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA11 Mar 2015
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA30 Jul 2014
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA26 Dec 2012
US
No image published for this recall

a product listed in the official notice - safety alert

High riskFDA20 Jul 2022
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA11 May 2022
US
No image published for this recall

ATTUNE Revision Tibial Augment Size 7/8 5mm- intended for knee joint replacement Part Code:152307001 - safety alert

Medium riskFDA13 Oct 2021

Weekly recall digest

Get next week's recalls before you need them.

One email every Monday — official-source recalls for your country, and nothing else. Unsubscribe from any email.

The digest is the slow lane — one email a week. For instant, severity-gated alerts the moment a notice is published, get the app.

This recall was published 19 Jan 2022. The next one won't wait for you to search.

RecallScope watches official sources for the brands and VINs you follow, and alerts you the moment a new notice is published.