L Perrigo recalls

L Perrigo appears in 28 official U.S. recall notices indexed by RecallRadar, most recently on 2023-07-19.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

Recall summary

Recalls

• Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a) 30-count cartons (NDC 0113-0847-39), and b) 45-count cartons (NDC 0113-0847-95),…
  FDA Drug · Class II · 2023-07-19 · L Perrigo
  Reason: Failed Impurities/Degradation Specifications
• Picnic, Fexofenadine Hydrochloride Tablets, 180 mg, Antihistamine, 90-count cartons, Distributed by: Thirty Madison, Inc., New York, NY 100…
  FDA Drug · Class II · 2023-07-19 · L Perrigo
  Reason: Failed Impurities/Degradation Specifications
• allergyrelief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a)30-count cartons (NDC 56062-847-39)
  FDA Drug · Class II · 2023-07-19 · L Perrigo
  Reason: Failed Impurities/Degradation Specifications
• Non-Drowsy Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, 150-count cartons, Distributed By: BJ's Wholesale Club, 25 Research…
  FDA Drug · Class II · 2023-07-19 · L Perrigo
  Reason: Failed Impurities/Degradation Specifications
• Allergy ALLER-FEX, Fexofenadine Hydrochloride Tablets, 180 mg, 180-count cartons, Packaged by: Perrigo, 515 Eastern Ave., Allegan, MI 49010…
  FDA Drug · Class II · 2023-07-19 · L Perrigo
  Reason: Failed Impurities/Degradation Specifications
• Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, 30-count cartons, Distributed By: CVS Pharmacy, Inc., One CVS Drive, Woonsocket…
  FDA Drug · Class II · 2023-07-19 · L Perrigo
  Reason: Failed Impurities/Degradation Specifications
• allergy relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a)15-count cartons (NDC 11673-617-22), b)30-count cartons (NDC 1167…
  FDA Drug · Class II · 2023-07-19 · L Perrigo
  Reason: Failed Impurities/Degradation Specifications
• Allergy, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a) 30-count cartons (NDC 72288-847-39), and b)150-count cartons (NDC 72288…
  FDA Drug · Class II · 2023-07-19 · L Perrigo
  Reason: Failed Impurities/Degradation Specifications
• allergy relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a)15-count cartons (NDC 79481-0847-0), b)30-count cartons (NDC 7948…
  FDA Drug · Class II · 2023-07-19 · L Perrigo
  Reason: Failed Impurities/Degradation Specifications
• aller-ease, Fexofenadine Hydrochloride Tablets, 180 mg, 30-count cartons, Packaged For: Your Military Exchanges, By: Perrigo Company, Alleg…
  FDA Drug · Class II · 2023-07-19 · L Perrigo
  Reason: Failed Impurities/Degradation Specifications
• Fexofenadine Hydrochloride Tablets, 180 mg, 100-count cartons, Distributed by: Perrigo, Allegan, MI 49010
  FDA Drug · Class II · 2023-07-19 · L Perrigo
  Reason: Failed Impurities/Degradation Specifications
• Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, 15-count cartons, Distributed By: Adusa Distribution, LLC, Salisbury, NC 28147
  FDA Drug · Class II · 2023-07-19 · L Perrigo
  Reason: Failed Impurities/Degradation Specifications
• Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a) 30-count cartons (NDC 36800-691-39), b)45-count cartons (NDC 368…
  FDA Drug · Class II · 2023-07-19 · L Perrigo
  Reason: Failed Impurities/Degradation Specifications
• Antacid Tablets, Calcium Carbonate chewable tablets, 750mg, 60-count bottle, OTC, [Healthy Accents brand NDC: 55316-014-72, Distributed by…
  FDA Drug · Class II · 2018-11-28 · L Perrigo
  Reason: Presence of foreign substance: Product found to contain metal particles.
• Scopolamine Transdermal Therapeutic System, 1 mg/3 days, a) 4-count (NDC 45802-580-84)
  FDA Drug · Class II · 2018-05-23 · L Perrigo
  Reason: Defective delivery system
• Maximum Strength Zephrex-D, Pseudoephedrine HCl, 30 mg, Nasal Decongestant. 24 softgel tablets per paper carton, Distributed by Perrigo, Al…
  FDA Drug · Class II · 2017-12-27 · L Perrigo
  Reason: Microbial Contamination of Non-Sterile Products
• Walgreens Daytime and Nighttime Cold & Flu, packaged in combo pack of two plastic 12FL OZ (355 mL) bottles connected by one paper sleeve, T…
  FDA Drug · Class III · 2017-07-05 · L Perrigo
  Reason: Labeling: Label Mix-Up - This product is being recalled due to an incorrect product sleeve on the product twin pack. The incorrect product sleeve is for Day-Night Cold and Flu whereas the batch contains Day-Night Coug…
• Option 2, Levonorgestrel Tablet, 1.5 mg, Emergency Contraceptive, 1 Tablet per box, Distributed By Perrigo, Allegan, MI 49010
  FDA Drug · Class II · 2017-06-14 · L Perrigo
  Reason: Defective Container: Carton is missing the tablet blister strip and tablet.
• Salicylic Acid Shampoo, 6%, 177 mL bottle, Rx only, Manufactured By Perrigo Yeruham, Israel, Distributed By Perrigo Allegan, MI 49010, NDC…
  FDA Drug · Class III · 2017-03-08 · L Perrigo
  Reason: Failed Impurities/Degradation Specifications: The API for these products had an out of specification result for an organic impurity.
• Salicylic Acid Cream, 6%, 400g bottle, Rx Only, Manufactured By Perrigo Yeruham, Israel 80500, Distributed By Perrigo Allegan, MI 49010, ND…
  FDA Drug · Class III · 2017-03-08 · L Perrigo
  Reason: Failed Impurities/Degradation Specifications: The API for these products had an out of specification result for an organic impurity.
• Clindamycin Phosphate and Benzoyl Peroxide Gel, 1.2%/5%, 45 g tubes, Rx Only, Manufactured by Perrigo, Yeruham, Israel, Distributed by Perr…
  FDA Drug · Class II · 2017-01-25 · L Perrigo
  Reason: Microbial Contamination of Non-Sterile Product; small number of tubes may include the presence of mold on the cap
• Acetaminophen suspension liquid, 160 mg/5 mL, dye-free grape flavor, 2 FL OZ (59 mL) bottle co-packaged with an oral dosing syringe in a ca…
  FDA Drug · Class II · 2013-11-27 · L Perrigo
  Reason: Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing syringe without dose markings.
• Acetaminophen suspension liquid, 160 mg/5 mL, grape flavor, 2 FL OZ (59 mL) bottle co-packaged with an oral dosing syringe in a carton and…
  FDA Drug · Class II · 2013-11-27 · L Perrigo
  Reason: Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing syringe without dose markings.
• Acetaminophen suspension liquid, 160 mg/5 mL, dye-free cherry flavor, co-packaged with an oral dosing syringe in a carton and sold under th…
  FDA Drug · Class II · 2013-11-27 · L Perrigo
  Reason: Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing syringe without dose markings.
• Acetaminophen suspension liquid, 160 mg/5 mL, cherry flavor, 2 FL OZ (59 mL) bottle co-packaged with an oral dosing syringe in a carton and…
  FDA Drug · Class II · 2013-11-27 · L Perrigo
  Reason: Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing syringe without dose markings.
• Liothyronine Sodium Tablets, USP, 5 mcg Rx ONLY, 100 count bottle, Distributed by: Paddock Laboratories, Inc., Minneapolis, MN 55427, NDC 0…
  FDA Drug · Class III · 2013-05-15 · L Perrigo
  Reason: Failed Impurities/Degradation Specifications: 3 month stability testing.
• PE Daytime Cold/Flu LiqGel, Multi Symptom Relief, Acetaminophen/Dextromethorphan HBr/Phenylephrine HCL 325/10/5 mg gel caps 20 count bliste…
  FDA Drug · Class III · 2013-04-03 · L Perrigo
  Reason: Subpotent; 12 month time point for the active ingredient Phenylephrine HCl.
• Prednisone tablets, USP, 10mg, Rx Only, Units of Use, NDC: a) 45802-303-67, 48-count Cartons, b) 45802-303-21, 21-count Cartons, Manufactur…
  FDA Drug · Class II · 2013-01-23 · L Perrigo
  Reason: 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 l…