Information on KinderFarms’ Voluntary Recall of KinderMed Pain & Fever Products

Effective immediately, KinderFarms is voluntarily recalling all of our KinderMed Pain & Fever products. This is the first time that the company has had to make this type of decision. KinderFarms continues to be guided by its mission to provide effective options that fit with our consumers values.

Right now, KinderFarms is working with the FDA to ensure that we complete this recall efficiently and completely.  If you have either KinderMed Infants’ or Kids’ Pain & Fever products, please discontinue use and return them to the store where you bought them.

Safety has always been the number one priority at KinderFarms, which is why we have stringent requirements for our products -- not only for the ingredients we use but for the rigorous testing in place to ensure our products are safe and meet high-quality standards.

While this issue only affects the KinderMed Infants’ and Kids’ Pain and Fever Products, KinderFarms is taking every step to further strengthen and enhance processes and testing across all of our products. No other KinderFarms products are impacted by this recall.

See the official press release below for information on this voluntary recall.

If you have any questions, please reach out to or 800-996-2930 from 6:00 AM to 5:00 PM (Pacific Time). 

KinderFarms values its relationship with parents and is dedicated to improving the wellbeing of all families. The company will continue to work hard to maintain your trust and ensure you have the utmost confidence in all KinderFarms product

Infant Pain and Fever
Kids Pain and Fever

KinderFarms, LLC Voluntarily Recalling All KinderMed Pain & Fever Products Due to Acetaminophen Instability

FOR IMMEDIATE RELEASE - November 13, 2023, Los Angeles, California – KinderFarms, LLC is voluntarily recalling all lots of KinderMed Infants’ Pain & Fever (oral suspension) and KinderMed Kids’ Pain & Fever (oral suspension) to the retail and consumer level. These products are being voluntarily recalled due to acetaminophen instability.  The two products were manufactured and packaged for KinderFarms by a major, U.S.-based OTC pharmaceutical manufacturer with over 30 years of experience. Ongoing testing of sample batches indicated some product lots were no longer in specification and may pose a health risk. Out of an abundance of caution, KinderFarms has made the decision to voluntarily recall all KinderMed Pain & Fever products.  

Acetaminophen is the active ingredient in many pain-relieving medicines. As a result of the potential health risk with acetaminophen being outside of specification, the product may cause acute adverse health effects, including abdominal pain, nausea, vomiting or jaundice at higher doses. The company has not received any reports of serious adverse events from either of these products to date. No other KinderFarms products are impacted by this recall. 

The impacted product being voluntarily recalled is all lots of:

  • KinderMed Infants’ Pain & Fever (2 fluid ounces/59 mL), (Acetaminophen - 160 mg per 5 mL), Oral Suspension UPC: 850001805698
  • KinderMed Kids’ Pain & Fever (4 fluid ounces/118 mL), (Acetaminophen - 160 mg per 5 mL), Oral Suspension UPC: 850001805728

This voluntary recall encompasses all product currently available on shelf of these two SKUs only. These products are available nationwide in drug/pharmacy, supermarkets, direct delivery and national retailers, and online through major ecommerce sites.

Consumers who purchased either of these two products should stop using them and may return the product to the place of purchase for a full refund. 

Consumers with questions may contact the company at or (800)-996-2930 from 6:00 AM to 5:00 PM (Pacific Time).

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

Complete and submit the report

Regular Mail or Fax: Download form or call 1-800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

For media inquiries, reach out to Aurora Gonzalez at