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Purdue Pharma, LP

Purdue Pharma, LP Recalls

All product recalls associated with Purdue Pharma, LP.

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Oct 2017

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–3 of 3 recalls

Betadine Solution Swabstick (Purdue) – packaging defect (2017)

Subpotent Drug: The laminate used to make the pouches was reversed such that the aluminum layer was in contact with the product causing an exothermic reaction between the free iodine and the aluminum.

Class IIModerate

FDAOct 5, 2017Nationwide• Purdue Pharma, LP

Intermezzo Sublingual Tablet (Purdue) – Dissolution Specs (2016)

Failed Dissolution Specifications

Class IIILow

FDAMar 31, 2016FL, LA, MI +5 more• Purdue Pharma L.P.

Intermezzo (Purdue Pharma) – dissolution failure (2015)

Failed dissolution specifications

Class IIILow

FDAJul 13, 2015Nationwide• Purdue Pharma L.P.