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L. Perrigo Company

L. Perrigo Company Recalls

All product recalls associated with L. Perrigo Company.

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Feb 2023

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 21–28 of 28 recalls

Clindamycin Benzoyl Peroxide Gel (Perrigo) – Mold Contamination (2016)

Microbial Contamination of Non-Sterile Product; small number of tubes may include the presence of mold on the cap

Class IIModerate

FDADec 28, 2016Nationwide• L. Perrigo Company

Acetaminophen Suspension Liquid (Perrigo) – defective syringe (2013)

Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing syringe without dose markings.

Class IIModerate

FDANov 1, 2013Nationwide• L. Perrigo Co.

Acetaminophen Suspension Liquid (Perrigo) – defective syringe (2013)

Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing syringe without dose markings.

Page 2 of 2Next

Class IIModerate

FDANov 1, 2013Nationwide• L. Perrigo Co.

Acetaminophen Suspension (L. Perrigo) – Defective Delivery System (2013)

Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing syringe without dose markings.

Class IIModerate

FDANov 1, 2013Nationwide• L. Perrigo Co.

Acetaminophen Suspension Liquid (Perrigo) – defective syringe (2013)

Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing syringe without dose markings.

Class IIModerate

FDANov 1, 2013Nationwide• L. Perrigo Co.

Liothyronine Tablets (Perrigo) – Stability Testing Failure (2013)

Failed Impurities/Degradation Specifications: 3 month stability testing.

Class IIILow

FDAMar 12, 2013Nationwide• L. Perrigo Co.

PE Daytime Cold/Flu LiqGel (L. Perrigo) – Subpotent Active Ingredient (2013)

Subpotent; 12 month time point for the active ingredient Phenylephrine HCl.

Class IIILow

FDAFeb 18, 2013AR, IN• L. Perrigo Co.

Prednisone Tablets (L. Perrigo Co) – Foreign Substance (2012)

Presence of Foreign Substance(s); Perrigo has been notified of a recall by the manufacturer of this product, West-Ward Pharmaceuticals. This is a sub-recall due to tablets contaminated with trace amounts of food-grade lubricant, as well as stainless steel inclusions

Class IIModerate

FDADec 17, 2012Nationwide• L. Perrigo Co.