# FDA recall D-0350-2022

> **Perrigo Company PLC** · Class II · drug recall initiated 2021-07-27.

## Product

TopCare Allergy Relief, Fexofenadine Hydrochloride tablets, 24HR, 180mg Antihistamine, packaged as a) 5 count bottle, NDC 36800-319-13 UPC 0 36800 33277-5 b)  15 count bottle, NDC 36800-319-22 UPC 0 36800 33278 2; c)  45 count bottle, NDC 36800-319-95 UPC 0 36800 33280-5; d)  90 count bottle, NDC 36800-319-75 UPC 0 36800 33282 9; Distributed Topco Associates LC, Elk Grove Village, IL 60007, Made in the Czech Republic,

## Reason for recall

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

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0350-2022
- **Recalling firm:** Perrigo Company PLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2021-07-27
- **Report date:** 2022-01-12
- **Termination date:** 2022-11-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Allegan, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0350-2022

## Citation

> AI Analytics. FDA recall D-0350-2022. Retrieved 2026-07-09 from https://api.ai-analytics.org/recall/D-0350-2022. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
