PlainRecalls
FDA Drug Moderate Class II Terminated

OCTREOTIDE ACETATE INJECTION, 50 mcg (base)/mL (0.05 mg/mL), 1 mL Single Dose Vial, Rx only, Manufactured by Fresenius Kabi USA, LLC, Schaumburg, IL 60173, NDC 63323-365-01.

Reported: June 1, 2016 Initiated: May 4, 2016 #D-0866-2016

Product Description

OCTREOTIDE ACETATE INJECTION, 50 mcg (base)/mL (0.05 mg/mL), 1 mL Single Dose Vial, Rx only, Manufactured by Fresenius Kabi USA, LLC, Schaumburg, IL 60173, NDC 63323-365-01.

Reason for Recall

Failed Impuities/Degradation Specifications

Details

Recalling Firm
Fresenius Kabi USA, LLC
Units Affected
355,150 vials
Distribution
Nationwide and Puerto Rico.
Location
Lake Zurich, IL

Frequently Asked Questions

What product was recalled?
OCTREOTIDE ACETATE INJECTION, 50 mcg (base)/mL (0.05 mg/mL), 1 mL Single Dose Vial, Rx only, Manufactured by Fresenius Kabi USA, LLC, Schaumburg, IL 60173, NDC 63323-365-01.. Recalled by Fresenius Kabi USA, LLC. Units affected: 355,150 vials.
Why was this product recalled?
Failed Impuities/Degradation Specifications
Which agency issued this recall?
This recall was issued by the FDA Drug on June 1, 2016. Severity: Moderate. Recall number: D-0866-2016.