# FDA recall D-0907-2018

> **LUPIN SOMERSET** · Class III · drug recall initiated 2018-06-13.

## Product

Equate ClearLAX, Polyethylene Glycol 3350 Powder for Solution, OS Osmotic Laxative, OTC, packaged in a) 119 g bottle (NDC 49035-312-07), b) 238 g bottle (NDC 49035-312-08), Distributed by: Wal-mart Stores, Inc., Bentonville, AR 72716

## Reason for recall

Labeling: Not Elsewhere Classified -  A private label distributor noted unfiled NDC numbers on EQ ClearLax Polyethylene Glycol 3350 NF Powder Solution of various sizes.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0907-2018
- **Recalling firm:** LUPIN SOMERSET
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-06-13
- **Report date:** 2018-07-11
- **Termination date:** 2021-02-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Somerset, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0907-2018

## Citation

> AI Analytics. FDA recall D-0907-2018. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-0907-2018. Source: US FDA. Licensed CC0.

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