RecallHawk

Airborne Gummies (63 and 75 count bottles)

RB Health (US) LLC ("Reckitt"), of Parsippany, New Jersey

Summary

CPSC recall: Airborne Gummies (63 and 75 count bottles). By RB Health (US) LLC ("Reckitt"), of Parsippany, New Jersey. Hazard: When opened for the first time, pressure build up in the bottle can cause the cap and underlying seal to pop off with force, posing an injury hazard.. Remedy: Consumers with an unopened bottle(s) should not attempt to open the product and should contact Reckitt to return the unopened bottle(s) to receive a full refund. A postage-paid label will be provided. Bottles that

Details

Source

CPSC Consumer Product Recall

External ID

9259

Action Date

2022-03-16

Status

Recalled

Category

consumer_product

Product Description

This recall involves only 63 and 75 count bottles of Airborne Gummies. They were sold in blueberry pomegranate, orange a

Context & Analysis

This is a unclassified recall.

This was one of 9 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

RB Health (US) LLC ("Reckitt"), of Parsippany, New Jersey has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

What is a FDA recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (RB Health (US) LLC ("Reckitt"), of Parsippany, New Jersey) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does RB Health (US) LLC ("Reckitt"), of Parsippany, New Jersey have FDA actions?

RB Health (US) LLC ("Reckitt"), of Parsippany, New Jersey has 2 FDA actions in our database, including 1 recall and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9259" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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