No image published for this recall

No image published for this recall

Aesculap Implant - safety alert

Official notice

25 Mar 2020

Last checked

25 Mar 2020

Medium riskFDA

An official FDA notice concerns Aesculap Implant - safety alert. An official FDA notice concerns Aesculap Implant. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2020-03-25. Recall numbers: Z-1478-2020. Check the official notice for the complete list. Published 2020-03-25.

What to do now

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

Units affected

24,010

Recall number

Z-1478-2020

Official notice

2020-03-25

The hazard

An official FDA notice concerns Aesculap Implant. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2020-03-25. Recall numbers: Z-1478-2020. 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.

Event Ids

84865

Recall Numbers

Z-1478-2020

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 · PA · Center Valley

Affected area 1

US · United States · PA · Center Valley

Affected area 2

US · United States

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Aesculap Implant. Contact: Aesculap Implant Systems LLC.

Source & status

Source

Tier

official

Category

ELECTRONICS

App estimate

medium

Recall details

Recall number

Z-1478-2020

Event id

84865

Units affected

24,010

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 riskFDA27 Jul 2022
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

Medium riskFDA27 Jul 2022
US
No image published for this recall

PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM Catalog Number: FC700SU - safety alert

Medium riskFDA6 Oct 2021
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA29 Sept 2021
US
No image published for this recall

proSA Tool Set used to adjust and verify the proSA Adjustable Shunt System Shunt, central nervous system and components - safety alert

Medium riskFDA7 Mar 2018
US
No image published for this recall

a product listed in the official notice - safety alert

Critical riskFDA21 Feb 2018
US
No image published for this recall

a product listed in the official notice - safety alert

Critical riskFDA24 May 2017
US
No image published for this recall

a product listed in the official notice - safety alert

Critical riskFDA19 Apr 2017
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA11 Jul 2012

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 25 Mar 2020. 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.