No image published for this recall

No image published for this recall

Maquet Cardiovascular Maquet Getinge-BO-T 41302 PRIMING LINES BUMC Material:701066291 - safety alert

Official notice

5 Jun 2019

Last checked

5 Jun 2019

Medium riskFDA

An official FDA notice concerns Maquet Cardiovascular Maquet Getinge-BO-T 41302 PRIMING LINES BUMC Material:701066291 - safety alert. An official FDA notice concerns Maquet Getinge-BO-T 41302 PRIMING LINES BUMC Material:701066291. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2019-06-05. Recall numbers: Z-1577-2019. Check the official notice for the complete list. Published 2019-06-05.

What to do now

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

Recall number

Z-1577-2019

Official notice

2019-06-05

The hazard

An official FDA notice concerns Maquet Getinge-BO-T 41302 PRIMING LINES BUMC Material:701066291. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2019-06-05. Recall numbers: Z-1577-2019. 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

82703

Recall Numbers

Z-1577-2019

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

Maquet Getinge-BO-T 41302 PRIMING LINES BUMC Material:701066291

Risk / hazard

An official FDA notice concerns Maquet Getinge-BO-T 41302 PRIMING LINES BUMC Material:701066291. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2019-06-05. Recall numbers: Z-1577-2019. 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 · NJ · Wayne

Affected area 1

US · United States · NJ · Wayne

Affected area 2

US · United States

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Maquet Cardiovascular. Contact: Maquet Cardiovascular, LLC.

Source & status

Source

Tier

official

Category

ELECTRONICS

App estimate

medium

Recall details

Recall number

Z-1577-2019

Event id

82703

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 riskFDA1 Oct 2025
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA24 Sept 2025
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA30 Apr 2025
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA23 Apr 2025
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA27 Nov 2024
US
No image published for this recall

a product listed in the official notice - safety alert

Critical riskFDA3 Jul 2024
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA13 Mar 2019
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA5 Nov 2014
US
No image published for this recall

VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500 - safety alert

Critical riskFDA6 Nov 2024
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA17 Jul 2024
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA24 Jan 2024
US
No image published for this recall

Acrobat-i Vacuum Positioner System, Model Number XP-5000Z - safety alert

Medium riskFDA27 Dec 2023

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 5 Jun 2019. 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.