Colorado recalls

Sold nationwide. Tzumi Electronics' SLF Sauna Blankets (model 30065TAR) can overheat during use, creating fire and burn risks. The company has received six reports of overheating, including five cases of minor furniture damage. About 3,600 units were sold through Target, Macy's, Snappy, and online from February 2025 through February 2026.

Serious·CPSC·May 28, 2026·Tzumi

Sold nationwide. Panasonic-branded VL2020 lithium coin batteries sold online were packaged in clear plastic bags without child-resistant packaging or required warning labels. If swallowed, coin batteries can cause serious internal burns and death within hours.

Serious·CPSC·May 28, 2026·Proudly American Store

Sold nationwide. Daoen Inc. is recalling Zen-branded magnetic ball fidget toys because the high-powered magnets inside can be swallowed by children. When multiple magnets are ingested, they can attract each other and become stuck in the digestive system, potentially causing serious internal injuries or death.

Serious·CPSC·May 28, 2026·Daoen

Sold nationwide. These small disc magnets are too powerful and too small, violating federal safety rules. If swallowed, multiple magnets can attract each other inside the stomach and intestines, causing perforations, blockages, and serious internal injury or death.

Serious·CPSC·May 28, 2026·MiniWarGaming Forge

Sold nationwide. The steam diffuser in these portable saunas can be positioned too close to your body, allowing hot steam to contact your skin. Giantex has received nine reports of burns, including one second-degree burn.

Serious·CPSC·May 28, 2026·Giantex

Sold nationwide. SkinnyDipped Dark Chocolate Coconut Almond Bites in certain lots may contain undeclared peanut or peanut butter, even though peanuts are not an intended ingredient. The issue was discovered after a consumer found peanut butter–containing products in the wrapper. People with peanut allergies could have a serious allergic reaction.

Moderate·FDA·May 27, 2026·Bazzini

Sold nationwide. Philips is recalling X-ray tube cooling units, type CU3101, that were made between February 2016 and May 2020. The deaeration hose may degrade and leak oil, which can reduce cooling. When oil flow drops too low, the system switches to low-dose fluoroscopy and shows a tube cooler message that restarting does not clear. The recall covers 3 product lines with about 5,000 affected units, and no injuries have been reported.

Moderate·FDA·May 27, 2026·Philips3 products

C.R. Bard has recalled certain Silastic Brand Foley Catheters (5cc and 30cc models) due to staining on the catheter surface. The affected catheters were distributed across the U.S. and Canada.

Moderate·FDA·May 27, 2026·Bard

Sold nationwide. Certain Philips Azurion fluoroscopy systems may experience mechanical wear in the Float Tabletop control, which could impair the longitudinal and transverse (side-to-side and front-to-back) movement of the examination table. This wear could affect the system's ability to position patients correctly during imaging procedures.

Moderate·FDA·May 27, 2026·Philips

Sold nationwide. Medtronic is recalling nine models of retrograde cannulas used in cardiopulmonary bypass procedures. Certain lots may have a sterile barrier that could be breached, which could compromise the product's sterility. No injuries have been reported.

Moderate·FDA·May 27, 2026·Medtronic9 products

Sold nationwide. The straight inserter tool on certain OneLIF Interbody Cage implants may fail to attach properly to the cage. This could prevent secure engagement during spinal fusion surgery, potentially causing procedural delays or requiring surgeons to choose a different implant.

Moderate·FDA·May 27, 2026·Novapproach Spine

Sold nationwide. ICU Medical oncology infusion kits with extension sets may develop leaks during chemotherapy administration. If a leak occurs during therapy, patients may receive less medication than intended, and healthcare workers or patients could be exposed to hazardous drugs.

Moderate·FDA·May 27, 2026·ICU Medical

Sold nationwide. Tangent Endoscopy's Single Use Digital Catheter (models TNG4002-IND and TNG-4007-6pk) can develop fractures at the tip of the shaft during use. While the fractured pieces have not completely detached in reported cases, a broken catheter tip could affect device function or potentially cause patient harm.

Moderate·FDA·May 27, 2026·Tangent Endoscopy

Sold nationwide. Becton Dickinson is recalling 3 Swan-Ganz catheter product lines, with 589,459 affected units in total. The blue proximal injectate lumen hub can leak or break because of manufacturing and material changes, which may lead to infection, medication loss, or blood loss. No injuries have been reported, and the products were distributed across the US and in many other countries.

Moderate·FDA·May 27, 2026·Becton Dickinson3 products

Sold nationwide. Sanfilippo is recalling six nut and trail mix products sold under the Southern Style Nuts, Squirrel Brand, Good & Gather and Fisher names because they may contain Salmonella. The products were distributed nationwide.

Serious·FDA·May 27, 2026·Southern Style Nuts6 products

Sold nationwide. PS Seasoning & Spices is recalling 6 products sold as Ellsworth Sour Cream + Onion Seasoning, Blackstone Parmesan Ranch Seasoning, 1P Original Smokehouse Unit, 1P Jalapeno Heat Unit, Save A Lot Bind, and Non Fat Dry Milk. The products were made with milk powder that its supplier recalled because of possible Salmonella contamination. The products were distributed nationwide, and no illnesses have been reported.

Serious·FDA·May 27, 2026·Ellsworth6 products

Llorens Pharmaceuticals is recalling Vitamin B-Complex, Vitamin C & Folic Acid dietary supplement (8 FL Oz bottles, Lot B2025, expiration 08/27) because some bottles contain black particulate matter. The contamination was identified before causing reported injuries.

Moderate·FDA·May 27, 2026·Llorens

Sold nationwide. Wellnov Supplements is recalling 14 products, including Joint Nourish, FulviLife Complex, Liposomal multivitamin drops, Liposomal Collagen Booster, Liposomal Kids Liquid Multivitamin Drops, and Liposomal D3, B12 and Sleep sprays. The products are made by VitaminAlly LLC in Chandler, Arizona, and were sold nationwide and in Puerto Rico. The FDA says manufacturing practices fell short in ways that could allow bacterial contamination and possible C. botulinum, and no illnesses have been reported.

Moderate·FDA·May 27, 2026·Joint Nourish14 products

Sold nationwide. Wisconsin Pharmacal Company's MG217 Multi-Symptom Treatment Cream (colloidal oatmeal 2%, 6 oz) has been found to contain Staphylococcus aureus bacteria. The contamination was confirmed in lot #1024088 (expiration 11/30/2026). About 690 tubes were distributed nationwide and to the Bahamas.

Serious·FDA·May 27, 2026·Wisconsin Pharmacal

Sold nationwide. IntegraDose Compounding Services LLC has recalled fentanyl citrate sterile injection (2,250 mcg/50 mL) because the drug may contain less active ingredient than labeled. This lot was distributed nationwide to healthcare facilities.

Moderate·FDA·May 27, 2026·IntegraDose

Sold nationwide. UCB Biosciences is recalling specific lots of Cimzia (certolizumab pegol) 200 mg prefilled syringes because the manufacturer cannot confirm the product remained sterile during production. This is a precautionary recall; no infections or injuries have been reported so far.

Moderate·FDA·May 27, 2026·UCB Biosciences

Sold nationwide. Zydus Pharmaceuticals is recalling erythromycin tablets (250 mg) due to the presence of N-Nitroso-Desmethyl-Erythromycin, a nitrosamine impurity, at levels above the FDA's acceptable intake limit. The affected bottles were distributed nationwide. This impurity can potentially increase cancer risk with long-term exposure.

Moderate·FDA·May 27, 2026·Zydus2 products

Sold nationwide. ANI Pharmaceuticals is recalling estradiol gel (0.1%, 0.25 mg packets) because some packets in affected cartons were found to be empty or only partially filled. This could mean patients receive less medication than prescribed. The recall affects carton lot M251109, which expires in November 2027.

Moderate·FDA·May 27, 2026·ANI Pharmaceuticals

Sold nationwide. Gas-X Simethicone 125 mg softgels distributed by Haleon are being recalled because the carton labeling does not list all inactive ingredients. This affects three specific lot codes (KB5Y, MP4B, and SS4F) distributed nationwide.

Moderate·FDA·May 27, 2026·Haleon

Sold nationwide. Lupin Pharmaceuticals is recalling certain batches of Liraglutide Injection (a diabetes and weight-loss medication) because white thread-like particles have been found inside the cartridges. The affected pens are distributed nationwide. No injuries have been reported.

Moderate·FDA·May 27, 2026·Lupin

Sold nationwide. Sagent Pharmaceuticals is recalling two lots of Busulfan Injection due to failed impurities and degradation specifications. The affected lots are 656412 (expiring 08/31/2026) and 659646 (expiring 03/31/2027). This is a prescription medication used in cancer treatment.

Moderate·FDA·May 27, 2026·Sagent Pharmaceuticals

Sold nationwide. Primidone tablets distributed by American Health Packaging were found to contain trace amounts of Acemetacin, a different active pharmaceutical ingredient, due to cross-contamination during manufacturing. The affected lot (1027583, expiring 09/30/2027) contains approximately 63,500 tablets distributed nationwide. No injuries have been reported.

Moderate·FDA·May 27, 2026·Amerisource2 products

Sold nationwide. Golden State Medical Supply is recalling Primidone 50 mg tablets because the active ingredient was contaminated with trace amounts of Acemetacin, a different medication. This contamination occurred during manufacturing. The affected bottles are identified by specific lot numbers with expiration dates in 2028.

Moderate·FDA·May 27, 2026·Golden State Medical Supply2 products

Sold nationwide. Lannett Company's Primidone Tablets 250mg were contaminated during manufacturing with trace amounts of Acemetacin, a different active pharmaceutical ingredient. The contamination affected specific lot numbers distributed nationwide. No injuries have been reported.

Moderate·FDA·May 27, 2026·Lannett

Sold nationwide. Insulet found a manufacturing issue in certain lots of Omnipod 5, Omnipod DASH, and Omnipod Eros pods that could cause insulin to leak instead of being fully delivered into the body. The leak occurs when a small tear develops in the tubing just above the skin. In some cases, users may not notice the problem, which can lead to high blood sugar levels and, in severe cases, diabetic ketoacidosis.

Serious·FDA·May 26, 2026·Omnipod