Perrigo Company PLC recalls
Every recall we track for Perrigo Company PLC — 106 in all, from 2015–2021 — plus the complaints and injury reports the public filed about them. 6 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Perrigo Company PLC peaked in 2021 (81); 101 since 2017. 5% rated “stop using now”.
All FDA recall records for Perrigo Company PLC since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 4 | 0 | 4 | 11 | 19 |
| 2020 | 0 | 0 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 32 | 48 | 81 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Perrigo Company PLC recalls before 2017
Recalls on record by year.
Most common reasons for Perrigo Company PLC recalls
What to do if you have a recalled Perrigo Company PLC product
- Match the NDC and lot number on your bottle or box to the recall.
- Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
- Report side effects to FDA MedWatch.
All Perrigo Company PLC recalls
9 shown- UnratedDrug
Perrigo Company PLC recalls No Drip Nasal Spray, Oxymetazoline HCl 0.05% Nasal Decongestant, 1 FL Oz (30 mL) per bottle, Distributed by SUPERVALU
Perrigo recalls nasal decongestant spray due to contaminated excipient. Products may pose health risks; check NDC 41163-703-10 and batch 1BK0964 for affected items.
PerrigoOct 26, 2021 - UnratedDrug
Perrigo Company PLC recalls GoodSense Aller.Ease, Fexofenadine hydrochloride 12 HR, 60 mg tablets, 24 count bottle, UPC 3 0113 0425 62 7; Made in
Perrigo Company PLC recalls GoodSense Aller.Ease 60mg tablets (UPC 3 0113 0425 62 7) after stability testing found impurity A. Consumers should check their bottles for lot numbers 0JE2487 or 0KE2982.
PerrigoJul 27, 2021 - Lower riskDrug
Perrigo Company PLC recalls Albuterol Sulfate Inhalation Aerosol, 90 mcg per actuation, 200 metered inhalations, Manufactured by: Catalent Pharma
Perrigo recalls Albuterol Sulfate Inhalers with defective delivery systems that may fail to dispense medication consistently. Affected units have specific NDC codes and expiration dates listed in the recall notice.
PerrigoSep 16, 2020 - UnratedDrug
Perrigo Company PLC recalls Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 80 tablets per bottle. [NDC: Brand] NDC Basic Care:
Perrigo Company PLC recalls 75mg Ranitidine tablets (NDCs listed) due to possible contamination with N-nitrosodimethylamine, a potential carcinogen. Consumers should contact the company for details.
PerrigoOct 23, 2019 - Stop using nowFood
Perrigo Company PLC recalls Parent's Choice Advantage Infant Formula Milk-Based Powder with Iron, 35 oz, 922 g, with UPC: 078742022468
Perrigo recalls Parent's Choice Advantage Infant Formula with possible metal fragments. Consumers should check UPC 078742022468 and lot code C26EVFV (use by Feb 26, 2021) for affected products.
PerrigoJun 20, 2019 - Lower riskFood
Perrigo Company PLC recalls Simple Truth Organic Banana, Strawberry & Apple Fruit Puree with Nonfat Greek Yogurt, 113 g, packed in a laminate
Perrigo recalls Simple Truth Organic Banana, Strawberry & Apple Fruit Puree with Nonfat Greek Yogurt due to improper labeling that fails to indicate milk content. This affects one lot (L8159) with best by date 08/06/2019.
PerrigoJan 21, 2019 - Use cautionDrug
Perrigo Company PLC recalls Nystatin, USP Powder for Rx compounding, 50 Million Units, Packaged by Perrigo, Minneapolis MN 55427, NDC 0574-0405-05,
Perrigo recalls Nystatin, USP Powder for Rx compounding due to a label error on declared strength. Check your lot number and expiration date.
PerrigoJan 18, 2016 - Stop using nowDrug
Perrigo Company PLC recalls Guaifenesin DM Cherry liquid (guaifenesin 100 mg/5 mL and Dextromethorphan HBr 5 mg/5 mL), packaged in 4oz. bottles,
Perrigo recalls several store-brand children's cough liquids due to incorrect dose markings on dosing cups. Check your bottles for lot numbers 5LK0528, 5LK0630, or 5LK0779.
PerrigoJan 8, 2016 - Lower riskDrug
Perrigo Company PLC recalls Cetirizine HCl 10 mg Tablet, 14 count blister packs, sold over the counter under the following brands, GoodSense brand
Perrigo recalls GoodSense and other store-brand Cetirizine HCl 10 mg tablets due to failed impurity specifications. Check your NDC and lot numbers.
GoodSenseSep 28, 2015
Perrigo Company PLC recall questions
How many recalls has Perrigo Company PLC had?
106 recalls from Perrigo Company PLC are on record with U.S. safety agencies, from 2015–2021 (104 drug, 2 food).
What is the most recent Perrigo Company PLC recall?
Perrigo Company PLC recalls No Drip Nasal Spray, Oxymetazoline HCl 0.05% Nasal Decongestant, 1 FL Oz (30 mL) per bottle, Distributed by SUPERVALU, dated Oct 26, 2021. Every Perrigo Company PLC recall is listed on this page, newest first.
Why are Perrigo Company PLC products recalled?
The most common reasons on record: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine. (17); Labeling: label error on declared strength. (2).
What should I do if I have a recalled Perrigo Company PLC product?
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
How do I get alerts for new Perrigo Company PLC recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.