foundmatterdb

Field reports on stuff that let you down

FDA recallMedicationsClass I· Fresenius Kabi USA, LLC

Tyenne (tocilizumab-aazg) Injection, 400 mg/20 mL (20 mg/mL), 20 mL vial, Rx Only, Manufa…

Official notice from a government agency or its published feed.

Tyenne (tocilizumab-aazg) Injection, 400 mg/20 mL (20 mg/mL), 20 mL vial, Rx Only, Manufactured by Fresenius Kabi USA, LLC, Lake Zurich, Illinois, 60047, NDC 65219-594-20.
Reason: Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles.
Class IThe FDA's most serious recall level: a reasonable chance the product could cause serious health problems or death. · Ongoing · Nationwide in the USA

Hazard: Presence of particulate matter:An internal investigation at the firm found the product to contain glass particles.

Seen this too? Add your take
Add a sticker (optional)Stick one on:
0/280