Recall Register

Food, drugs, devices › Perrigo Company PLC

Food recall: Simple Truth Organic Banana, Strawberry & Apple Fruit Puree with Nonfat Greek Yogurt, 113 g, packed in a laminate pouch,

FDA enforcement event 81966 · Class II · initiated 21 Jan 2019 · status Terminated · terminated 21 May 2019

FoodVoluntary: Firm initiated1 product recordAllegan, MI

FDA enforcement event 81966 is a food recall by Perrigo Company PLC of Allegan, MI, initiated 21 Jan 2019 and classified Class II, with 1 product record.

FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 56% of the 516 food enforcement events initiated in 2019 carry the same class.

Status: Terminated, terminated 21 May 2019. Initiation: voluntary: firm initiated. Perrigo Company PLC has 9 enforcement events on this register, with a median of 2 product records per event.

Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.

Recalling firm

Perrigo Company PLC, Allegan, MI.

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 Greek Yogurt, LOT L8159, best by 08/06/2019 due to improper labeling that does not indicate the presence of milk."

Distribution

"Domestic: Alabama, Arkansas, Georgia, Illinois, Indiana, Kentucky, Louisiana, Michigan, Missouri, Mississippi, Ohio, South Carolina, Tennessee, Texas, Virginia, and West Virginia. No…"

Product records

Recall numberProductQuantityClassStatusReport date
F-1155-2019Simple Truth Organic Banana, Strawberry & Apple Fruit Puree with Nonfat Greek Yogurt, 113 g, packed in a laminate pouch, Each case has 6 cartons with 6 pouches per carton. Total of 36 pouches per case.106,632 pouches.Class IITerminated20 Mar 2019

Context

56%of 2019 food events are Class II516 events that year
1product record in this eventfirm median: 2
9events on this register for the firm

Other enforcement events for Perrigo Company PLC

InitiatedProduct (first record)TypeClassRecords
26 Oct 2021Acetaminophen Oral Suspension Grape Flavor, 160 mg per 5 mL, 16 fl oz (473 mL) per bottle, Distributed by Perrigo, AllegDrugClass II51
27 Jul 2021EQUALINE aller-ease fexofenadine hydrochloride tablets, 180 mg, 24 HR, packaged as a) 15 count bottle, NDC 41163-571-22,DrugClass II30
16 Sep 2020Albuterol Sulfate Inhalation Aerosol, 90 mcg per actuation, 200 metered inhalations, Manufactured by: Catalent Pharma SoDrugClass II1
23 Oct 2019Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 30 tablets per bottle. [NDC: Brand] NDC CVS Health: 69842-DrugClass II17
20 Jun 2019Parent's Choice Advantage Infant Formula Milk-Based Powder with Iron, 35 oz, 922 g, with UPC: 078742022468FoodClass II1
18 Jan 2016Nystatin, USP Powder for Rx compounding, 50 Million Units, Packaged by Perrigo, Minneapolis MN 55427, NDC 0574-0405-05, DrugClass II2
8 Jan 2016Guaifenesin Grape liquid 100 mg/5 mL, packaged in 4oz. bottles, co-packaged with a dosing cup in a carton and sold underDrugClass II2
28 Sep 2015Cetirizine HCl 10 mg Tablet, 14 count blister packs, sold over the counter under the following brands, GoodSense brand dDrugClass III1

All 9 events for Perrigo Company PLC

Questions and answers

Why was this food recalled?

FDA's record gives the reason for recall as: "Perrigo Company is initiating a voluntary recall of one production lot of Simple Truth Organic Banana, Strawberry and Apple Fruit Puree with Nonfat Greek Yogurt, LOT L8159, best by 08/06/2019 due to improper labeling that does not indicate the presence of milk."

What does Class II mean?

FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.

Where was the product distributed?

FDA's distribution pattern field reads: "Domestic: Alabama, Arkansas, Georgia, Illinois, Indiana, Kentucky, Louisiana, Michigan, Missouri, Mississippi, Ohio, South Carolina, Tennessee, Texas, Virginia, and West Virginia. No…"

Is the recall still ongoing?

FDA lists the status as Terminated; the termination date is 21 May 2019. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.

Where does this data come from?

openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.

Provenance

Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.