FDAClass IIJuly 31, 2019

Gericare Diocto Liquid Docusate Sodium Stool Softener recall: CGMP Deviations

Gericare Diocto Liquid Docusate Sodium Stool Softener, 50 mg/5mL, 16 FL OZ (473 ml), Dist. BY: Gericare Pharmaceuticals corp. 1650 63rd Street…

Why was Gericare Diocto Liquid Docusate Sodium Stool Softener recalled?

cGMP Deviations: Products may have microbial contamination.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot #: 70612, Exp 6/19

Product
Gericare Diocto Liquid Docusate Sodium Stool Softener, 50 mg/5mL, 16 FL OZ (473 ml), Dist. BY: Gericare Pharmaceuticals corp. 1650 63rd Street…
Recalling firm
Geritrex, LLC
Quantity
6165 bottles
Distribution
U.S.A. Nationwide
Recall date
July 31, 2019
Classification
Class II
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls