Children's Acetaminophen Suspension Recalled for Failed Impurity Specifications
KinderFarms is recalling KinderMed KIDS' PAIN & FEVER Acetaminophen oral suspension nationwide due to failed impurity and degradation specifications that do not meet FDA standards.
The agency’s classification
FDA (Drugs): Class II
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.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: FDA Class II recall of a children's medication with failed impurity and degradation specifications represents a risk-of-harm product. No illnesses or injuries have been reported, keeping the score at maximum 3 per the rubric.
Plain-English summary
KinderFarms LLC is recalling KinderMed KIDS' PAIN & FEVER Acetaminophen oral suspension due to failed impurities and degradation specifications. The product is a children's over-the-counter pain and fever reducer distributed in 4 FL OZ bottles with Organic Cherry Flavor.
The recall involves approximately 591,684 bottles distributed nationwide across multiple lot numbers, with expiration dates ranging from August 2024 to August 2025. The product did not meet FDA specifications for impurities and degradation, indicating potential quality defects in the formulation.
Consumers who have obtained this product should refer to the recall notice for specific lot numbers and expiration dates. Those with questions about the safety of this product should consult a healthcare provider or contact KinderFarms LLC.
The recalled product
- Product
- PAIN AND FEVER (ACETAMINOPHEN)
- Brand
- PAIN AND FEVER
- Manufacturer
- KINDER FARMS LLC
- Category
- Drug — Children's OTC Medication
- Hazard
- Affected units
- 591,684
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- 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
UPCs (2)
- 0850001805728
- 850001805728
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 2 recalled by KINDER FARMS LLC under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 2 products in this recall →Related recalls
Same brand · PAIN AND FEVER
- ModerateL. Perrigo Recalls Infants' Pain and Fever Acetaminophen Due to Dosing Syringe Defect
FDA (Drugs) · 2013-11-27
- ModerateL. Perrigo Recalls Infants' Acetaminophen Suspension Due to Dosing Syringe Markings
FDA (Drugs) · 2013-11-27
Same manufacturer · KINDER FARMS LLC
See all →- HighKinderFarms Infants' Acetaminophen Recalled for Failed Impurity and Degradation Standards
FDA (Drugs) · 2023-12-13
Same hazard · impurities
See all →- ModerateCipla Recalls Fosfomycin Tromethamine Due to Impurity Specification Failures
FDA (Drugs) · 2026-10-14
- LowSun Pharmaceutical Recalls Tretinoin Cream Due to Impurity Failures
FDA (Drugs) · 2026-10-14
- LowSun Pharmaceutical Recalls Tretinoin Cream Due to Impurity Failures
FDA (Drugs) · 2026-10-14
- LowSun Pharmaceutical Recalls Tretinoin Cream Due to Impurity Specifications
FDA (Drugs) · 2026-10-14
- LowMacleods Recalls Olanzapine Tablets Due to Impurity Levels
FDA (Drugs) · 2026-09-30
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