# FDA recall D-1550-2016

> **Mckesson Packaging Services** · Class III · drug recall initiated 2016-09-08.

## Product

Lansoprazole Delayed-Release Capsules, USP, 30 mg, packaged in 100-count cartons of 10 x 10 unit dose blister cards, Rx only, Manufactured by: Dr. Reddy's Laboratories, Inc., 200 Somerset Corporate Blvd Floor 7, Bridgewater, NJ 08807, NDC 63739-0555-10

## Reason for recall

Labeling: Label mix-up. The inner packaging was properly labeled Omeprazole DR 40mg Capsules, but the outer secondary packaging was mislabeled Lansoprazole Delayed-Release 30mg Capsules.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1550-2016
- **Recalling firm:** Mckesson Packaging Services
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-09-08
- **Report date:** 2016-10-05
- **Termination date:** 2017-05-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Concord, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1550-2016

## Citation

> AI Analytics. FDA recall D-1550-2016. Retrieved 2026-05-24 from https://api.ai-analytics.org/recall/D-1550-2016. Source: US FDA. Licensed CC0.

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