Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Fresenius Kabi USA LLC (FK USA)

Fresenius Kabi USA LLC (FK USA) Recalls

All product recalls associated with Fresenius Kabi USA LLC (FK USA).

Get alerts for this brand

Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Feb 2013

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–2 of 2 recalls

Calcium Gluconate Injection (Fresenius) – Missing Label (2013)

Labeling: Missing label

Class IIILow

FDAFeb 1, 2013Nationwide• Fresenius Kabi USA LLC (FK USA)

Irinotecan Injection (Fresenius) – Crystallization Issue (2013)

Crystallization: Active pharmaceutical ingredient is precipitating in product solution.

Class IIModerate

FDAJan 22, 2013Nationwide• Fresenius Kabi USA LLC (FK USA)