Generic drug makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in IrelandLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list L. Perrigo Company with 28 drug recalls and 24 drug applications. The most recent is a drug recall dated Nov 1, 2013: Acetaminophen suspension liquid, 160 mg/5 mL, dye-free grape flavor, 2 FL OZ (59 mL) bot….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Nov 1, 2013 | 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 carClass II · Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing | Drug recalls |
| Nov 1, 2013 | 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 Class II · Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing | Drug recalls |
| Nov 1, 2013 | Acetaminophen suspension liquid, 160 mg/5 mL, dye-free cherry flavor, co-packaged with an oral dosing syringe in a carton and sold under theClass II · Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing | Drug recalls |
| Nov 1, 2013 | 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 sClass II · Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing | Drug recalls |
| Mar 12, 2013 | Liothyronine Sodium Tablets, USP, 5 mcg Rx ONLY, 100 count bottle, Distributed by: Paddock Laboratories, Inc., Minneapolis, MN 55427, NDCClass III · Failed Impurities/Degradation Specifications: 3 month stability testing. | Drug recalls |
| Feb 18, 2013 | PE Daytime Cold/Flu LiqGel, Multi Symptom Relief, Acetaminophen/Dextromethorphan HBr/Phenylephrine HCL 325/10/5 mg gel caps 20 count blisteClass III · Subpotent; 12 month time point for the active ingredient Phenylephrine HCl. | Drug recalls |
| Dec 17, 2012 | Prednisone tablets, USP, 10mg, Rx Only, Units of Use, NDC: a) 45802-303-67, 48-count Cartons, b) 45802-303-21, 21-count Cartons, ManufactureClass II · Presence of Foreign Substance(s); Perrigo has been notified of a recall by the manufacturer of this product, West-Ward P | Drug recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
