Recall archive
11 recalls · page 1 of 1
Reported Aug 8, 2024
Perrigo Company plc recalls CVS Health, H-E-B Baby Premium Infant Formula with Iron Milk-Based Powder due to Product contains levels of Vitamin D above the…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Perrigo Company PLC
Matched: Brand · Product — Product contains levels of Vitamin D above the maximum level permitted
FDA (recalls & safety alerts)
Reported Mar 17, 2023
Perrigo Company plc recalls Gerber Good Start Powdered Infant formula due to Potential Cronobacter sakazakii contamination
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Perrigo Company PLC
Matched: Brand · Product — Potential Cronobacter sakazakii contamination
FDA (recalls & safety alerts)
Reported Mar 2, 2022
Acetaminophen Oral Suspension Grape Flavor, 160 mg per 5 mL, 16 fl oz (473 mL) per bottle, Distributed by Perrigo,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Perrigo Company PLC
Matched: Brand · Product · Product details — CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
50 more products in this recall
FDA (openFDA drug enforcement)
Reported Jan 12, 2022
EQUALINE aller-ease fexofenadine hydrochloride tablets, 180 mg, 24 HR, packaged as a) 15 count bottle, NDC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Perrigo Company PLC
Matched: Brand — Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
29 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 30, 2020
Albuterol Sulfate Inhalation Aerosol, 90 mcg per actuation, 200 metered inhalations, Manufactured by: Catalent Pharma…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Perrigo Company PLC
Matched: Brand · Product details — Defective Delivery System: Sustained trend of failure to dispense complaints.
FDA (openFDA drug enforcement)
Reported Mar 25, 2020
Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 30 tablets per bottle. [NDC: Brand] NDC CVS Health:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Perrigo Company PLC
Matched: Brand — CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
16 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 24, 2019
Parent's Choice Advantage Infant Formula Milk-Based Powder with Iron, 35 oz, 922 g, with UPC: 078742022468
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Perrigo Company PLC
Matched: Brand — Product may contain metal fragments.
FDA (openFDA food enforcement)
Reported Mar 20, 2019
Simple Truth Organic Banana, Strawberry & Apple Fruit Puree with Nonfat Greek Yogurt, 113 g, packed in a laminate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Perrigo Company PLC
Matched: Brand · Reason for recall — Perrigo Company is initiating a voluntary recall of one production lot of Simple Truth Organic Banana, Strawberry and Apple Fruit Puree with Nonfat…
FDA (openFDA food enforcement)
Reported Feb 10, 2016
Nystatin, USP Powder for Rx compounding, 50 Million Units, Packaged by Perrigo, Minneapolis MN 55427, NDC 0574-0405-05,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Perrigo Company PLC
Matched: Brand · Product · Product details — Labeling: label error on declared strength.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Feb 3, 2016
Guaifenesin Grape liquid 100 mg/5 mL, packaged in 4oz. bottles, co-packaged with a dosing cup in a carton and sold…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Perrigo Company PLC
Matched: Brand — Defective Delivery System: Firm recalled Guaifenesin liquid and Guaifenesin DM liquid due incorrect dose markings on the dosing cups.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Dec 30, 2015
Cetirizine HCl 10 mg Tablet, 14 count blister packs, sold over the counter under the following brands, GoodSense brand…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Perrigo Company PLC
Matched: Brand · Product details — Failed Impurity/Degradations Specifications; impurity identified as cetirizine monosaccharide ester
FDA (openFDA drug enforcement)
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