Poly Pharmaceuticals, Inc. Recalls

Overview of recall records associated with Poly Pharmaceuticals, Inc., including dates, categories and classifications where available.

2recall records

Jul 23, 2014latest record date

Jul 23, 2014earliest record date

Recall history in this database

Classification mix: Class III: 2.

DrugJul 23, 2014

Poly Pharmaceuticals LORTUSS EX, Each 5 mL (1 teaspoonful) contains: Codeine Phosphate 10 recall — FDA D-1432-2014

Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below monograph specifications, and label inaccurately contains wording "Rx Only".

Class IIIFDA: TerminatedPoly Pharmaceuticals, Inc.

DrugJul 23, 2014

Poly Pharmaceuticals POLY-TUSSIN AC LIQUID, Each 5 mL (1 teaspoonful) contains recall — FDA D-1431-2014

Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below monograph specifications, and label inaccurately contains wording "Rx Only".

Class IIIFDA: TerminatedPoly Pharmaceuticals, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Poly Pharmaceuticals, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.