FDA recall D-0907-2018

LUPIN SOMERSET · Class III · drug

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

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

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