News

November 28, 2023

Recalled Cinnamon Applesauce Pouches Causing High Blood Lead Levels in Children

Various recalled cinnamon apple purée and applesauce products with elevated lead levels have been reported to the U.S. Food and Drug Administration (FDA). The recalled products have been the cause of 52 reported cases of illness in children, as of November 22.

The Centers for Disease Control and Prevention (CDC) has issued a Health Alert Network (HAN) Health Advisory to advise clinicians and health departments to report cases to their local health authorities.

Background

FDA, CDC, and state and local partners are investigating a potential link between high blood lead levels and consuming certain cinnamon-containing apple purée and applesauce products.

State partners tested multiple lots of the reported products, and test results indicated the products contained extremely high levels of lead. WanaBana, Schnucks, and Weis have initiated voluntary recalls of certain lots of the following products:

  • WanaBana brand apple cinnamon fruit purée pouches
  • Schnucks brand cinnamon applesauce pouches
  • Weis brand cinnamon applesauce pouches

More Information

More information about the specific recalled products may be found on the FDA’s website: Investigation of Elevated Lead Levels: Applesauce Pouches (November 2023) | FDA

News

June 27, 2023

June Recalls on Children’s Products

Parents and caregivers should be aware of several child-related product recalls.

Learn More

Here is a list of June recalls collected from the following major federal agencies: the Consumer Product Safety Commission, the Food and Drug Administration, and the National Highway Traffic Safety Administration.

More Information

For recall details, visit the links above or review the Consumer Product Safety Commission, the Food and Drug Administration and the National Highway Traffic Safety Administration websites.

News

April 24, 2023

April Recalls on Children’s Products

Parents and caregivers should be aware of several child-related product recalls.

Learn More

Here is a list of April recalls collected from the following major federal agencies: the Consumer Product Safety Commission, the Food and Drug Administration, and the National Highway Traffic Safety Administration.

More Information

For recall details, visit the links above or review the Consumer Product Safety Commission, the Food and Drug Administration and the National Highway Traffic Safety Administration websites.

News

July 16, 2020

FDA Warning: Hand Sanitizers Containing Methanol

About

On July 2, the U.S. Food & Drug Administration (FDA) issued a warning that there has been a sharp increase in hand sanitizer products labeled to contain ethanol (a.k.a. ethyl alcohol) but have tested positive for methanol contamination. Methanol, or wood alcohol, is a substance that can be toxic when absorbed through the skin and toxic or life-threatening when ingested.

Understanding the Risk

Methanol is not an acceptable active ingredient for hand sanitizers and must not be used due to its toxic side effects. The FDA is aware of instances where adults and children ingested contaminated hand sanitizers that have led to blindness, hospitalization, and death. The FDA’s investigation of methanol in certain hand sanitizers is still ongoing.

Risks are especially high for young children who accidentally ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute. Please do not ingest any type of hand sanitizer, regardless of whether or not it is contaminated with methanol.

Receiving Medical Attention

Individuals exposed to hand sanitizers containing methanol who are experiencing symptoms should seek immediate treatment for potential methanol poisoning. Substantial exposure to methanol can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system, or death.

If you need to report adverse events or quality problems experienced with the use of hand sanitizers, contact the FDA’s MedWatch Adverse Event Reporting program online or through a printable form that can be submitted via fax at 1.800.332.0178.

More Information

A list of hand sanitizer products to avoid can be found on the FDA website. For more information, see the full update.

News

February 3, 2020

Recall Issued on More Than 165,000 Infant Incline Sleepers

The U.S. Consumer Product Safety Commission (CPSC), along with four other companies, issued a recall on more than 165,000 infant incline sleepers due to a risk of suffocation.

About

According to the CPSC, the following companies have been impacted by the recall: Summer Infant, Graco, Delta Enterprises Corp., and Evenflo. The recall was issued due to reported infant fatalities after “the infants rolled from their back to their stomach or side, or under other circumstances” while using an infant incline sleeper. The CPSC urges consumers to immediately stop using the products listed below and to contact the companies to learn more about refund options.

Recalled Products

Recalled products include:

More Information

To learn more, read the full WTAE article.

*Information provided by WTAE