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Siemens ADVIA Centaur BNP (B-type Natriuretic Peptide), Catalog Numbers: 02816138 (100 tests), 02816634 (500 tests) - safety alert

Official notice

13 Jun 2018

Last checked

13 Jun 2018

Medium riskFDA

An official FDA notice concerns Siemens ADVIA Centaur BNP (B-type Natriuretic Peptide), Catalog Numbers: 02816138 (100 tests), 02816634 (500 tests) - safety alert. An official FDA notice concerns ADVIA Centaur BNP (B-type Natriuretic Peptide), Catalog Numbers: 02816138 (100 tests), 02816634 (500 tests). The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2018-06-13. Lots: ending. Recall numbers: Z-2053-2018. Check the official notice for the complete list. Published 2018-06-13.

What to do now

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

Units affected

21,687

Recall number

Z-2053-2018

Official notice

2018-06-13

The hazard

An official FDA notice concerns ADVIA Centaur BNP (B-type Natriuretic Peptide), Catalog Numbers: 02816138 (100 tests), 02816634 (500 tests). The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2018-06-13. Lots: ending. Recall numbers: Z-2053-2018. 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

ending

Event Ids

79496

Recall Numbers

Z-2053-2018

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Affected products

Product 1

ADVIA Centaur BNP (B-type Natriuretic Peptide), Catalog Numbers: 02816138 (100 tests), 02816634 (500 tests)

Units affected

21,687

Risk / hazard

An official FDA notice concerns ADVIA Centaur BNP (B-type Natriuretic Peptide), Catalog Numbers: 02816138 (100 tests), 02816634 (500 tests). The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2018-06-13. Lots: ending. Recall numbers: Z-2053-2018. 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 · NY · Tarrytown

Affected area 1

US · United States · NY · Tarrytown

Affected area 2

US · United States

Company & contacts

Brand

Manufacturer

Not provided

Phone

Not provided

Brand: Siemens. Contact: Siemens Healthcare Diagnostics, Inc..

Source & status

Source

Tier

official

Category

ELECTRONICS

App estimate

medium

Recall details

Recall number

Z-2053-2018

Event id

79496

Units affected

21,687

Status

active

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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