No image published for this recall

No image published for this recall

Cardiovascular - safety alert

Official notice

31 May 2017

Last checked

31 May 2017

Medium riskFDA

An official FDA notice concerns Cardiovascular - safety alert. An official FDA notice concerns Cardiovascular. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2017-05-31. Lots: 92254. Recall numbers: Z-2122-2017. Check the official notice for the complete list. Published 2017-05-31.

What to do now

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

Units affected

1,396

Recall number

Z-2122-2017

Official notice

2017-05-31

The hazard

An official FDA notice concerns Cardiovascular. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2017-05-31. Lots: 92254. Recall numbers: Z-2122-2017. 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

92254

Event Ids

76953

Recall Numbers

Z-2122-2017

Checked manually this time?

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

Turn on recall alerts

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 · MN · Saint Paul

Affected area 1

US · United States · MN · Saint Paul

Affected area 2

US · United States

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Cardiovascular. Contact: Cardiovascular Systems Inc.

Source & status

Source

Tier

official

Category

ELECTRONICS

App estimate

medium

Recall details

Recall number

Z-2122-2017

Event id

76953

Units affected

1,396

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

Medium riskFDA19 Sept 2018
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA14 Feb 2018
US
No image published for this recall

a product listed in the official notice - safety alert

Critical riskFDA1 Apr 2015
US
No image published for this recall

a product listed in the official notice - safety alert

Critical riskFDA20 Aug 2014
US
No image published for this recall

a product listed in the official notice - safety alert

Low riskFDA5 Mar 2014
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA19 Apr 2017
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA18 Jul 2012
US
No image published for this recall

WIRION EMBOLIC PROTECTION SYSTEM, Delivery Catheter and Filter and Retrieval Catheter, 6Fr, REF (Model Number) WRN-D6 - safety alert

Critical riskFDA29 Dec 2021
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA6 Jul 2016

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 31 May 2017. 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.