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Fresenius Kabi - safety alert

Official notice

4 Dec 2013

LowFDA

An official FDA notice concerns Fresenius Kabi. The notice reports a potential product safety risk. Follow the official notice for consumer instructions. Published 2013-12-04. Lots: 871ZA00201, 871ZA00301, 871ZA00302, 871ZA00401, 871ZA00402 and 5 more. Recall numbers: D-016-2014. Check the official notice for the complete list.

What to do now

Instructions for consumers are available in the official FDA notice.

Units affected

71,129

Recall number

D-016-2014

Official notice

2013-12-04

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

871ZA00201, 871ZA00301, 871ZA00302, 871ZA00401, 871ZA00402, 872ZA00101, 872ZA00201, 872ZA00301, 872ZA00401, 872ZA00501

Event Ids

66810

Recall Numbers

D-016-2014

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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

Affected area 1

US · United States

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Fresenius Kabi. Contact: Fresenius Kabi USA, LLC.

Source & status

Source

Tier

official

Category

HEALTH

Classification

Class III

App estimate

low

Recall details

Recall number

D-016-2014

Event id

66810

Units affected

71,129

Status

terminated

Classification

Class III

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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