Key Takeaway

EQUALINE aller-ease fexofenadine hydrochloride tablets, 180 mg, 24 HR, packaged as a) 15 count bottle, NDC 41163-571-22, UPC 0 41163 48067 4; b) 70 tablets per bottle, NDC 41163-571-01, UPC 0 41163 49 by Perrigo Company PLC was recalled on July 27, 2021. The hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.

FDA Drug Class II Terminated

EQUALINE aller-ease fexofenadine hydrochloride tablets, 180 mg, 24 HR, packaged as a) 15 count bottle, NDC 41163-571-22, UPC 0 41163 48067 4; b) 70 tablets per bottle, NDC 41163-571-01, UPC 0 41163 49

Recalled: July 27, 2021 ~55,032 units units affected D-0328-2022

Description

EQUALINE aller-ease fexofenadine hydrochloride tablets, 180 mg, 24 HR, packaged as a) 15 count bottle, NDC 41163-571-22, UPC 0 41163 48067 4; b) 70 tablets per bottle, NDC 41163-571-01, UPC 0 41163 49847 1; Made in the Czech Republic, Distributed by: UNFI Providence, RI 02908.

Hazard / Reason

Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.

Class II: Product that may cause temporary or medically reversible health consequences.

Class II indicates the product may cause temporary or medically reversible health effects. The probability of serious harm is considered remote.

Products Affected

EQUALINE aller-ease fexofenadine hydrochloride tablets, 180 mg, 24 HR, packaged as a) 15 count bottle, NDC 41163-571-22, UPC 0 41163 48067 4; b) 70 tablets per bottle, NDC 41163-571-01, UPC 0 41163 49

Drugs

Company Information

Perrigo Company PLC

Allegan, MI, United States

View all 106 recalls by Perrigo Company PLC →

Distribution

Nationwide in the USA

Related Recalls

Frequently Asked Questions

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