Philadelphia personal injury attorneys say Johnson & Johnson has recalled 200,000 bottles of Concentrated Motrin Infants’ Drops. Concentrated Infants’ MOTRIN® Drops The Department advises parents who have the recalled MOTRIN Infants Drops to return them to the place of purchase for a full refund. The FDA Alert(s) below may be specifically about Motrin Infant Drops or relate to a group or class of drugs which include Motrin Infant Drops (ibuprofen).MedWatch Safety Alerts are distributed by the FDA and published by Drugs.com.

Out of an abundance of caution, McNeil is voluntarily recalling the three lots released to the market made with the same batch of active ingredient.Healthcare professionals and patients are encouraged to report adverse events or side effects related to the use of these products to the FDA's MedWatch Safety Information and Adverse Event Reporting Program:McNeil Consumer Healthcare and FDA notified healthcare professionals of a voluntary recall of certain over-the-counter (OTC) Children's and Infants' liquid products manufactured in the United States, including The names of the products and manufacturers that received warning letters are: * The lack of adequate data on the cardiovascular safety of long-term use of Bextra, along with the increased risk of adverse cardiovascular (CV) events in short-term coronary artery bypass surgery (CABG) trials that FDA believes may be relevant to chronic use.
All Rights Reserved. Motrin drops for infants recalled due to plastic contamination A brand of ibuprofen for children that is used to alleviate pain and fever were recalled by manufacturer Johnson & Johnson (J&J) after it was discovered to have been contaminated with tiny plastic bits, according to a … Language + Settings bottles. Please see our Fort Washington, PA (September 6, 2013)  -  McNeil  Consumer  Healthcare  Division  of McNEIL-PPC, Inc. (“McNeil”) is voluntarily recalling at the retail level three lots, approximately 200,000 bottles, of Concentrated MOTRIN® Infants’ Drops Original Berry Flavor 1/2 fl oz bottles distributed in the United States (see full product list below). Infant ’ s Advil Concentrated Drops Grape acetic acid, artificial flavors, butylated hydroxytoluene, carboxymethylcellulose sodium, citric acid monohydrate, edetate disodium, FD&C blue no. * Lack of any demonstrated advantages for Bextra compared with other NSAIDs.Patients currently taking Bextra should contact their physicians to consider alternative treatments. Some of the features on CT.gov will not function properly with out javascript enabled. This lot was not released to the market. ET, Monday through Friday.If consumers have questions regarding this recall or to report an adverse event, please contact the Pfizer Consumer Healthcare Information Line at 1-800-88-Advil (1-800-882-3845).

HALF However, it is important to carefully weigh the benefits and risks of using prescription and OTC pain medicines during pregnancy. How We’re Mobilizing Our Resources to Help Find Solutions for COVID-19 McNeil Consumer Healthcare Announces Voluntary Recall of Three Lots of Concentrated MOTRIN® Infants Drops Original Berry Flavor 1/2 fl ozMcNeil Consumer Healthcare Announces Voluntary Recall of Three Lots of Concentrated MOTRIN® Infants Drops Original Berry Flavor 1/2 fl oz 40, glycerin, microcrystalline cellulose, polysorbate 80, propylene glycol, purified water, sodium benzoate, sorbitol solution, sucrose, xanthan gum

Please see our HALF We want to keep you aware of potential food poisonings to protect you and your loved ones from serious health issues. While mail and phone calls will be processed as quickly as possible, we recommend using our online services, or sending an email to the appropriate division/person instead. Before having surgery, tell your doctor or dentist about all the products you use (including prescription drugs, nonprescription drugs, and herbal products). Concentrated Infants’ MOTRIN® Drops Dye-Free Berry Flavor 1 fl oz is not included in this recall. Batch # / UPC: Various. For more information, please visit Pfizer Consumer Healthcare, a division of Pfizer Inc., is voluntarily recalling one lot of Pfizer concluded that the use of the product with an unmatched dosage cup marked in teaspoons rather than milliliters has a chance of being associated with potential overdose.


FDA is also asking manufacturers of all marketed prescription NSAIDs, including Celebrex (celecoxib), a COX-2 selective NSAID, to revise the labeling (package insert) for their products to include a boxed warning and a Medication Guide. Its most recent series of recalls began in April 2010 after more than 136 million children and infant over-the-counter medicines were recalled.

The company has provided questions and answers on For the latest FDA MedWatch alerts, Infants already susceptible to the adverse effects of ibuprofen may be at a slightly higher risk if they receive medication from an impacted bottle. Children’s or Adult MOTRIN® products are not included in this recall. This site is governed solely by applicable U.S. laws and governmental regulations. If you have any questions or concerns, or would like to inquire about a refund, please call our Consumer Care Center at 1-877-414-7709. After releasing these three lots of infants’ drops, the company found tiny plastic particles about the size of a poppy seed in a subsequent lot. The Medication Guide will accompany every prescription NSAID at the time it is dispensed to better inform patients about the CV and GI risks. The lot number and UPC codes are typically printed on the outside packaging and on the printed bottle label.The potential for adverse medical events related to the reason for this recall is not likely.