# FDA recall D-0811-2016

> **Apace KY LLC** · Class III · drug recall initiated 2016-02-12.

## Product

Minocycline Hydrochloride Capsules USP, 100 mg*, 30 Capsules (3 x 10) Unit Dose blisters (NDC 50268-569-11, barcode 5026856911) per carton (NDC 50268-569-13, barcode 5026856913), Rx only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478.

## Reason for recall

Labeling: Incorrect or Missing Lot and/or Exp Date: the individual blisters are mislabeled with an incorrect lot number of 13560 rather than the correct lot number of 13650.

## Distribution

All product was shipped to KY and further distributed Nationwide

## Key facts

- **Recall number:** D-0811-2016
- **Recalling firm:** Apace KY LLC
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-02-12
- **Report date:** 2016-04-13
- **Termination date:** 2016-08-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Fountain Run, KY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0811-2016

## Citation

> AI Analytics. FDA recall D-0811-2016. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-0811-2016. Source: US FDA. Licensed CC0.

---

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