Baby swabs and nasal swabs recalled for possible fungus in swab parts
That's what manufacturer Church & Dwight said in its notice announcing the recall of Orajel Baby Teething Swabs, Zicam Cold Remedy Nasal Swabs and Zicam Nasal AllClear Swabs from stores across the United States, including Puerto Rico.
The lots and expiration dates involved? All.
READ MORE: Recalled UTI drug could have deadly microbial contamination
What can contaminated swabs do?
Swabs with a microbial contamination can cause 'serious and life-threatening blood infections in users whose nasal mucosa may be compromised due to inflammation and mechanical injurie,' the recall notice states. 'The risk is highest (potentially severe or life-threatening) among children and individuals with compromised immune systems or other underlying medical conditions.'
Exactly which Orajel and Zicam swabs are recalled?
▪ Zicam Cold Remedy Nasal Swabs carry UPC No. 732216301205.
▪ Zicam Nasal AllClear Swabs, which were discontinued in December, carry UPC No. 732216301656.
▪ Orajel baby swabs carry UPC No. 310310400002.
What should you do now?
If you have the swabs, throw them in the trash or, for a refund, reach out go Church & Dwight either online or by calling 800-981-4710. Questions can be directed to that phone number, 9 a.m. to 5 p.m., Monday through Friday.
If you think you or your baby is having a medical issue caused by these swabs, go see a medical professional. Then, notify the FDA's MedWatch Adverse Event Program, either by filling out a form online or by requesting a reporting form at 800-332-1088.
Then, third, call Church & Dwight.
Hashtags
Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles
Yahoo
9 minutes ago
- Yahoo
Azurity Pharmaceuticals, Inc. Announces the Availability of BRYNOVIN™ (sitagliptin), the First and Only Oral Liquid Sitagliptin
WOBURN, Mass., July 31, 2025 /PRNewswire/ -- Azurity Pharmaceuticals, Inc. announced today the availability of BRYNOVIN™ (sitagliptin) oral solution, a dipeptidyl peptidase-4 (DPP-4) inhibitor indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. BRYNOVIN is not recommended in patients with type 1 diabetes and has not been studied in patients with a history of pancreatitis. BRYNOVIN, which was approved by the U.S. Food and Drug Administration (FDA) in January 2025, is the first and only oral liquid sitagliptin for the management of type 2 diabetes mellitus in adults in conjunction with diet and exercise.1 "BRYNOVIN demonstrates our commitment to breaking down barriers to patient care by providing sitagliptin in an oral liquid solution for adult patients with T2DM that may have difficulty swallowing pills or may have needle fear that affects treatment adherence," said Ron Scarboro, CEO at Azurity Pharmaceuticals. "Building on our longstanding legacy in dose form innovations, we continue to rapidly grow our capabilities in this space and deliver on our purpose to serve overlooked patients." With more than 38 million Americans living with diabetes2, and 90-95% of them diagnosed with type 2 diabetes, there remains a significant need for alternative treatment options3. For many, especially older adults and those in long-term care facilities, swallowing pills is a daily challenge that may lead to poor adherence and compromised outcomes4,5. BRYNOVIN provides effective HbA1c control as an adjunct to diet and exercise when used as monotherapy or in combination with other antihyperglycemic agents in adults with type 2 diabetes mellitus. The recommended dose of BRYNOVIN is 100 mg (25 mg/mL), administered as 4 mL once daily. BRYNOVIN is not recommended in patients with type 1 diabetes and has not been studied in patients with a history of pancreatitis. For full prescribing information, please visit 1. U.S Food and Drug Administration Orange Book. Accessed July 21, 2025. Centers for Disease Control and Prevention (CDC). Type 2 Diabetes. Accessed July 17, 2025 Centers for Disease Control and Prevention (CDC). National Diabetes Statistics Report 2024. https:// Wittenberg E, et al. "Medication Adherence in Older Adults: A Qualitative Study." Patient Preference and Adherence. 2019;13:1443–1450.5. Schiele J et al "Difficulties swallowing solid oral dosage forms in a general practice population: prevalence, causes, and relationship to dosage forms" Eur J Clinical Pharmacol (2013) 69:937-948 About Azurity Pharmaceuticals:Azurity Pharmaceuticals is a privately held company committed to delivering innovative, high-quality medicines for overlooked patients. Azurity's global footprint is over 50 countries, with a diversified portfolio of 50+ medicines spanning 10 dosage forms and 10 key therapeutic areas. Powered by its Next-Gen Commercial Model, Azurity leverages data, analytics, and AI-driven digital tools to enhance market reach and stakeholder engagement. Our medicines have benefited millions of people. For more information, including prescribing information, visit ©2025 Azurity Pharmaceuticals, Inc. PP-BRN-US-0029 View original content to download multimedia: SOURCE Azurity Pharmaceuticals
Entrepreneur
10 minutes ago
- Entrepreneur
Celsius Energy Drink May Contain Alcohol in Labeling Mixup
Don't drink your afternoon Celsius at work this week without checking the label first. If you're about to crack open a cold can of Celsius Astro Vibe energy drink, Sparkling Blue Razz Edition, with a silver top, you might want to put it back in the fridge. A major labeling mix-up of popular alcoholic seltzers and popular energy drinks has led to a recall, according to a safety notice posted to the FDA website. In what is basically a TikTok parody come true, alcoholic seltzer company High Noon said that beach-themed variety packs were mistakenly mislabeled as Celsius, a popular energy drink that does not contain alcohol (but does contain 270 mg of caffeine per can). Related: Liquid Death Announces a 'Sane' Energy Drink: 'The Category Has Gone a Little Caffeine-Crazy' "The recall was initiated after High Noon discovered that a shared packaging supplier mistakenly shipped empty Celsius cans to High Noon," the FDA statement reads. The affected cans were shipped to retailers between July 21 and 23 in Florida, Michigan, New York, Ohio, Oklahoma, South Carolina, Virginia, and Wisconsin. Celsius customers can check their labels for the exact recall codes. "Consumption of the liquid in these cans will result in unintentional alcohol ingestion," the notice says. No illnesses or adverse events have been reported for this recall to date, it adds. A spokeswoman for High Noon told the New York Times in an email that the incident affects only a "small batch" but did not give a number. Related: 'Consumers Deserve Better': How Superstar QB Patrick Mahomes Is Brewing a Better Future for Coffee Drinkers "We are working with the [FDA] retailers, and distributors to proactively manage the recall to ensure the safety and well-being of our consumers," the spokesperson told the outlet. The maximum amount of caffeine that's considered safe for healthy adults is 400 mg a day, according to the Mayo Clinic. Join top CEOs, founders and operators at the Level Up conference to unlock strategies for scaling your business, boosting revenue and building sustainable success.
Miami Herald
23 minutes ago
- Miami Herald
Popular energy drink pulled from shelves for containing vodka
We all have been there. We enter the store to grab a few basic groceries, only to find out that the products we bought have expired. The majority of people can relate to this because of our fast-paced world, where we don't take time to shop patiently and examine the products. Though I have a habit of only checking dairy products' expiration dates while in the store, these are not the only products that can go bad. Don't miss the move: Subscribe to TheStreet's free daily newsletter How do expired products end up on the shelves? While it is the responsibility of store workers to examine product expiration dates and remove expired products, sometimes they are so swamped with work that they don't have time to do it, or they miss something in a hurry. This year, multiple worker strikes occurred across various supermarkets and retail giants in the country. One of the main reasons for strikes was understaffing. Large companies often think only about profits, so they don't want to hire enough workers to cover every task required. Instead, they try to save on salaries and maximize their own gains. Sometimes, accidents happen in the manufacturing facilities. To err is human, but it is important to correct mistakes before anyone gets hurt, which can easily happen in the food industry. Earlier this month, Kraft Heinz issued a major recall over the possible contamination of turkey bacon with the hazardous bacteria Listeria monocytogenes. Now, one huge energy drink brand is recalling its products for another mishap. The FDA announced Tuesday that High Noon is recalling two production lots of High Noon Beach Variety packs (12-packs/12 fluid-ounce cans). Some of these packs ended up with cans containing High Noon Vodka seltzer alcohol, mislabeled Celsius Astro Vibe Energy Drink, Sparkling Blue Razz Edition, with a silver top. Related: Delta Air Lines blasted for possibly ripping off passengers Consuming a Celsius drink from one of these packs will result in unintentional alcohol ingestion. While the ingestion of a little bit of vodka might sound like fun for many, it is essential to remember that there are people with health conditions who can't tolerate alcohol. Then there are people with alcohol use disorder, for whom a single drink can pose a serious threat of relapse. In addition, some people don't drink for religious reasons. This labeling error is confined to the two lots listed below: High Noon Beach Variety Packs (12-pack and 12 fluid ounce cans with silver lids) with the following lots: L CCC 17JL25 14:00 to L CCC 17JL25 23:59 and L CCC 18JL25 00:00 to L CCC 18JL25 03:00. CELSIUS ASTRO VIBE Energy Drink, Sparkling Blue Razz Edition (12 fluid ounce cans with silver lids, instead of black) with the following lots: L CCB 02JL25 2:55 to L CCB 02JL25 3:11. The recall is only for the affected High Noon Beach Variety 12-packs with the listed lot codes that were shipped to distributors in Florida, Michigan, New York, Ohio, Oklahoma, South Carolina, Virginia, and Wisconsin. Related: Danone recalls YoCrunch because it might kill you Distributors shipped products to retailers across Florida, New York, Ohio, South Carolina, Virginia, and Washington between July 21 and July 23. Even though consumers might not have purchased a High Noon Beach Variety pack, the companies advise them to ensure their Celsius Astro Vive Energy Drink, Sparkling Blue Razz Edition doesn't show the noted lot codes before consuming. More Retail: Supermarket inflation: Beef prices soar as egg prices fallLevi's shares plan to beat tariffs, keep holiday prices downAmazon's quiet pricing twist on tariffs stuns shoppers The companies stressed that consumers are advised to dispose of Celsius Astro Vive Energy Drink, Sparkling Blue Razz Edition with silver lids and impacted lot codes and not consume the drink. Consumers should also reach out to High Noon consumer relations (consumerrelations@ to get more information and refunds. Recall key takeaways: A silver lid instead of a black one should be red flag; Consumers are advised not to drink from cans with impacted lot codes;Consumers should dispose of these cans and contact the High Noon consumer relations team for refunds. The Arena Media Brands, LLC THESTREET is a registered trademark of TheStreet, Inc.
