PlainRecalls
FDA Drug Critical Class I Terminated

Phenylephrine HCl, 1 mg in Sterile Water for Injection, QS 10mL Injectable Solution, 1 mg/10 mL incorrectly labeled as (10 mcg per mL), 10 mL syringe, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, (877) 794-0404; NDC: 42852-802-61.

Reported: January 2, 2019 Initiated: November 29, 2018 #D-0347-2019

Product Description

Phenylephrine HCl, 1 mg in Sterile Water for Injection, QS 10mL Injectable Solution, 1 mg/10 mL incorrectly labeled as (10 mcg per mL), 10 mL syringe, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, (877) 794-0404; NDC: 42852-802-61.

Reason for Recall

Labeling: Label Error on Declared Strength: Label incorrectly lists concentration as "10 mcg per mL" rather than the correct concentration of "100 mcg per mL".

Details

Recalling Firm
Advanced Pharma Inc.
Units Affected
225 syringes
Distribution
Heath care facilities in NM, TX, and OH
Location
Houston, TX

Frequently Asked Questions

What product was recalled?
Phenylephrine HCl, 1 mg in Sterile Water for Injection, QS 10mL Injectable Solution, 1 mg/10 mL incorrectly labeled as (10 mcg per mL), 10 mL syringe, Rx only, Avella of Houston, 9265 Kirby Dr., Houston, TX 77054, (877) 794-0404; NDC: 42852-802-61.. Recalled by Advanced Pharma Inc.. Units affected: 225 syringes.
Why was this product recalled?
Labeling: Label Error on Declared Strength: Label incorrectly lists concentration as "10 mcg per mL" rather than the correct concentration of "100 mcg per mL".
Which agency issued this recall?
This recall was issued by the FDA Drug on January 2, 2019. Severity: Critical. Recall number: D-0347-2019.