PlainRecalls
FDA Drug Low Class III Terminated

Clonidine HCL Injection, 1000 mcg/10mL (100 mcg/mL), 10 ML Single Dose Vial, Rx only, Manufactured for: X-Gen Pharmaceuticals, Big Flats, NY 14814, NDC 39822-2000-1.

Reported: April 17, 2019 Initiated: March 29, 2019 #D-1084-2019

Product Description

Clonidine HCL Injection, 1000 mcg/10mL (100 mcg/mL), 10 ML Single Dose Vial, Rx only, Manufactured for: X-Gen Pharmaceuticals, Big Flats, NY 14814, NDC 39822-2000-1.

Reason for Recall

Labeling: Label Error on Declared Strength: Side carton panel incorrectly lists the concentration as "500 mcg Clonidine Hydrochloride" rather than the correct concentration of "100 mcg Clonidine Hydrochloride" per mL.

Details

Units Affected
24,966 vials
Distribution
Nationwide in the USA.
Location
Horseheads, NY

Frequently Asked Questions

What product was recalled?
Clonidine HCL Injection, 1000 mcg/10mL (100 mcg/mL), 10 ML Single Dose Vial, Rx only, Manufactured for: X-Gen Pharmaceuticals, Big Flats, NY 14814, NDC 39822-2000-1.. Recalled by X-Gen Pharmaceuticals Inc.. Units affected: 24,966 vials.
Why was this product recalled?
Labeling: Label Error on Declared Strength: Side carton panel incorrectly lists the concentration as "500 mcg Clonidine Hydrochloride" rather than the correct concentration of "100 mcg Clonidine Hydrochloride" per mL.
Which agency issued this recall?
This recall was issued by the FDA Drug on April 17, 2019. Severity: Low. Recall number: D-1084-2019.