CLASS II ONGOING Drug recall · Reported 13 Dec 2023 · FDA Enforcement Report

KinderMed Kids' Pain & Fever Acetaminophen, 160 mg recalled

Kinder Farms is recalling KinderMed Kids' Pain & Fever Acetaminophen, 160 mg per, Oral Suspension, Organic Cherry, distributed nationwide in the US. The recall was initiated on 13 Nov 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot: CJ70900, CJ76796, Exp: 8/2024; CJ77051, Exp: 09/2024; WK02998, WK02997, WK04390, WK02999, Exp: 10/2024; WK03716, Exp:12/2024; WK05150, WK05151, WK07174, Exp:02/2025; WK05539, WK06534, Exp: 03/2025; WK10259, WK23040, Exp: 04/2025; WK27455, Exp: 08/2025.

NDC82673-097

UPC0850001805728, 850001805728

Quantity recalled591,684 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number: D-0142-2024
FDA event ID: 93448
Recalling firm: Kinder Farms, Redondo Beach, CA
Brand: Pain And Fever
Manufacturer: KinderFarms, LLC
Classification: Class II
Status: Ongoing
Recall initiated: 13 Nov 2023
FDA classified: 6 Dec 2023
Reported: 13 Dec 2023
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Potency & Assay
Drug class: Pain Medication

Timeline

13 Nov 2023	Recall initiated by company
6 Dec 2023	Classified by FDA	+23 days
13 Dec 2023	Published in enforcement report	+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Failed Impurities/Degradation Specifications

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

KinderMed KIDS' PAIN & FEVER Acetaminophen, 160 mg per 5 mL bottles, Oral Suspension, Organic Cherry Flavor, 4 FL OZ (118 mL), Distributed By: KinderFarms, Redondo Beach, CA 90277, NDC 82673-097-04, UPC 850001805728.

Where it was distributed

Nationwide

Questions about this recall

Why was it recalled?

Failed Impurities/Degradation Specifications

Which lots are affected?

Lot: CJ70900, CJ76796, Exp: 8/2024; CJ77051, Exp: 09/2024; WK02998, WK02997, WK04390, WK02999, Exp: 10/2024; WK03716, Exp:12/2024; WK05150, WK05151, WK07174, Exp:02/2025; WK05539, WK06534, Exp: 03/2025; WK10259, WK23040, Exp: 04/2025; WK27455, Exp: 08/2025.

Where was it sold?

Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 93448

This product is part of a recall event; the main page for the event is KinderMed Infants' Pain & Fever Acetaminophen, 160 mg recalled.

Reported	Class	Recall	Company	Reason	Where
13 Dec 2023	CLASS II	KinderMed Infants' Pain & Fever Acetaminophen, 160 mg recalledInfants Pain And Fever	Kinder Farms	Potency & Assay	Nationwide

More recalls from Kinder Farms

All 2

Reported	Class	Recall	Company	Reason	Where
13 Dec 2023Drug	CLASS II	KinderMed Infants' Pain & Fever Acetaminophen, 160 mg recalledInfants Pain And Fever	Kinder Farms	Potency & Assay	Nationwide

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