Search Cosmetics & Toiletries

183 Results

Unilever U.S. is recalling these products out of an abundance of caution. Unilever has received no reports of adverse events to date relating to this recall.

Unilever Recalls Dry Shampoos for Possible Elevated Benzene Levels

Dove, Nexxus, Suave, TIGI (Rockaholic and Bed Head) and TRESemmé dry shampoos are among the brands cited for concerns.

Henkel is conducting this voluntary recall with the knowledge of the U.S. Food and Drug Administration.

Henkel Recalls Alterna Bond Repair Leave-in Heat Protection Spray

Henkel has so far received no reports of harm or injury in connection with this product.

Recall Reminder: Test Products

Routine product tests initiated this product recall--a harsh reminder of the importance of testing and preserving products.

Kanebo Recalls Brightening Products Containing Rhododenol

Kanebo Cosmetics Inc. and its affiliates Lissage Ltd. and E’quipe, Ltd. have recalled brightening products from the Japanese market containing the quasi-drug ingredient rhododenol (4-(4-hydroxyphenyl)-2-butanol).

ProductRecallTextPaperTorn850

Facing a Recall? The FDA Offers Advice

In order for a recall to be effective, timely (and as painless as possible), it’s crucial that companies be prepared to take all necessary steps once it is initiated. The U.S. FDA is drafting a guidance to help.

HandSanitizerBlackJackerBackgroundHumanHands_850x425

20 Hand Sanitizers Recalled by Health Canada

Health Canada has recalled 20 hand sanitizers between March 31, 2021, and June 22 for ingredient violations, unauthorized sale and more, adding to nearly 100 previous recalls, CTV News reports.

The sunscreen spray products are packaged in aerosol cans.

Edgewell Recalls Banana Boat Hair & Scalp Sunscreen Due to Benzene

Banana Boat will also offer reimbursement for consumers who have purchased a product marked with one of the lot codes affected.

Dreamstime M 215000140

P&G Detects Benzene in Antiperspirant and Body Sprays, Issues Recall

P&G has voluntarily recalled specific lots of Old Spice and Secret aerosol spray antiperspirants and Old Spice Below Deck aerosol spray products due to the detection of benzene.

Product-Recall-850x425

FDA Begins Expediting Recall Information

The agency is increasing transparency in the product recall process.

Chattem Recalls Icy Hot Products

Chattem Inc. has initiated a voluntary nationwide recall of its Icy Hot Heat Therapy products, including consumer "samples" that were included on a limited promotional basis in cartons of its 3 oz. Aspercreme product...

L'Oréal Voluntarily Recalls Blonde Bleach

L'Oréal Paris, a division of L'Oréal USA, has initiated a voluntary recall from retail stores in the United States for the L'Oréal Paris Dream Blonde Bleach and Lightening care kit.

Foaming Scrub Lot Recalled Due to Bacteria Presence

Arbonne International LLC has voluntarily recalled a lot of Seasource Detox Spa Foaming Sea Salt Scrub due to the presence of Pseudomonas aeruginosa.

claires_425

UPDATE: Claire's Recalls Glitter Cosmetics After Asbestos Allegations

Claire's, a retailer aimed at young girls and teenagers, has recalled several glitter-containing products after allegations surfaced that they contain asbestos.

FDA Recalls Face Paint Due to Adverse Reactions

The FDA has learned of a cluster of adverse events in children exposed to various colors of the face paint. All exposures occurred on the same day at an organized event and included rashes, itchiness, burning sensation, and swelling where the face paints were applied.

Non-acetone Nail Polish Remover

FDA Recalls Nail Polish Remover After Burn Reports

The US Food and Drug Administration (FDA) has issued a statement recalling of Non-Acetone Nail Polish Remover due to a possible health risk.

Company Recalls Acne Gels Due to Bacteria Threat

The company recalled 1 ounce (28 g) tubes of DG Maximum Strength Acne Medicated Gel, sold at Dollar General; Kroger Acne Gel 10% Benzoyl Peroxide Acne Medication, sold at Kroger; and Equate: Medicated Acne Gel, sold at Wal-Mart.

The inner packaging of a serum and product kit containing said serum listed SPF when the product has no SPF.

FDA Flags Color Additive, SPF and Contaminant Offenses, Urges 'Recall Readiness'

In recent months, the U.S. Food and Drug Administration (FDA) reported six voluntary recalls for an impermissible color additive, mislabeled SPF and several contaminants. It also urged companies to be "recall ready" and provided final guidance to do so.

Wherefour Tool

Wherefour Traceability Tool Eases Recalls, Audits

Wherefour, Inc. has designed a traceability tool to allow quicker decision-making with cloud-based, tagged document storage functions to help make compliance and record-keeping easier.

Page 1 of 11