Alaska recalls

Sold nationwide. Nipro is recalling four hemodialysis concentrate products because they may contain high levels of endotoxin, a substance from bacteria. The recall covers about 13,000 cases and 100 drums across the US, Guatemala, and Panama, with US distribution in FL, GA, IL, MD, MI, NC, NJ, NV, OH, PA. No injuries have been reported.

Serious·FDA·Sep 16, 2026·Nipro4 products

Sold nationwide. HeartSine Technologies has recalled certain models of the SAM 350P, SAM 360P, and SAM 450P public access defibrillators (PADs) due to a damaged membrane component that can cause an intermittent electrical fault. The fault could prevent the device from operating properly when needed in a cardiac emergency. Approximately 11,912 affected units have been identified by serial number.

Serious·FDA·Sep 16, 2026·HeartSine

Sold nationwide. Bard is recalling six Foley and intermittent catheter tray products because the pericare wipes packed with them may have contamination on their surface. The recall followed customer complaints, and no injuries have been reported. The trays were distributed across the United States and in several other countries.

Moderate·FDA·Sep 16, 2026·Bard6 products

Sold nationwide. Atrium Medical is recalling three Getinge PVC thoracic catheter products, covering 11 model sizes, from a single lot. Testing found bacterial endotoxin levels above the allowed limit. No injuries have been reported.

Moderate·FDA·Sep 16, 2026·Atrium Medical3 products

Sold nationwide. Lutronic's DermaV laser system may produce sparks and loud noise when used at higher energy levels (fluences) at the 1064 nm wavelength with current cooling settings. This spark hazard could result in patient burns during treatment.

Moderate·FDA·Sep 16, 2026·Lutronic

Sold nationwide. Halyard IV Start Kit Non-Sterile (REF: KRIV26-02) convenience kits contain BD ChloraPrep Clear and FREPP Clear applicators with wrinkles in the paper lidding that may breach the seal. This compromises sterility assurance of the applicators. 98 kits in lot 1658438 (expiration 7/31/2026) were distributed nationally.

Moderate·FDA·Sep 16, 2026·AVID MedicalExpanded Sep 30

Sold nationwide. The Bravo CF capsule delivery device is used during esophageal pH monitoring procedures to attach a small capsule to the esophagus. The capsule may fail to attach properly or detach from the delivery device during use. This can result in the capsule being inhaled, perforating the esophagus, blocking the airway, or causing bleeding.

Serious·FDA·Sep 16, 2026·Given Imaging

Sold nationwide. L-Nutra Inc's Prolon Everyday Apulian Almond & Cocoa Spread contains undeclared hazelnut, cashew, and pistachio allergens. The product was sold online nationwide in 8-ounce glass jars (Lot L2755, expiring January 2, 2027).

Moderate·FDA·Sep 16, 2026·Prolon

Sold nationwide. Momchipz Gluten Free Veggie Chips (Broccoli Florets & Cauliflower, 3 oz) contain undeclared wheat, which is not listed on the package label. The product was sold in the U.S. and imported from Indonesia. People with celiac disease or wheat allergy are at risk.

Serious·FDA·Sep 16, 2026·Momchipz

Sold nationwide. B. Braun Medical Inc. is recalling specific lots of 0.9% Sodium Chloride Injection due to the presence of particulate matter, including iron oxide, inorganic material, cellulose fibers, and polystyrene. The contamination was identified during quality testing. This is a sterile injectable product distributed nationwide.

Serious·FDA·Sep 16, 2026·B. Braun

Sold nationwide. American Regent's epinephrine injection (1 mg/mL, 30 mL vials) may contain particulate matter—including nylon, glass, and other materials—and some vials are broken or leaking. This affects the sterility and safety of the medication. Three specific lot numbers distributed nationwide are involved.

Serious·FDA·Sep 16, 2026·American Regent

Sold nationwide. OurPharma LLC's fentanyl citrate 1,000 mcg injection solution has conflicting expiration dates printed on the IV bag and product labeling. The bag shows expiry dates of 07/31/2026 or 11/30/2026, while the product itself is labeled as expiring 12/09/2026. This discrepancy could lead to confusion about when the medication is safe to use.

Moderate·FDA·Sep 16, 2026·OurPharma

Sold nationwide. Baxter Healthcare identified stainless steel particles in certain 2000 mL bags of Dextrose Injection, USP 70%. The contamination affected 606 bags (Lot #Y495066, expiration July 31, 2027) distributed nationwide. No injuries have been reported.

Serious·FDA·Sep 16, 2026·Baxter

Sold nationwide. Ajanta Pharma USA Inc. is recalling fluphenazine hydrochloride 1mg tablets (NDC 27241-255-01) because stability testing at 18 months found organic impurity levels slightly above specification limits. The tablets contained 1.1% of Impurity-A, exceeding the 1.0% specification. No injuries have been reported.

Moderate·FDA·Sep 16, 2026·Ajanta Pharma

Sold nationwide. ImprimisRx NJ LLC is recalling specific lots of Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution used in medical offices because the medication contains lower-than-intended active ingredients. The affected lots may not work as intended for their intended use.

Moderate·FDA·Sep 16, 2026·ImprimisRx

Sold nationwide. So Delicious Dairy Free® Salted Caramel Cluster Non-Dairy Frozen Dessert pints may contain small stones or other hard objects in the cashew pieces. The issue was found through customer complaints. Affected pints have best-by dates on or before April 3, 2028.

Moderate·FDA·Sep 15, 2026·So Delicious

Sold nationwide. Gias Foods is recalling two lots of Bettergoods Authentic Italian Lemon Alfredo Fettuccine frozen pasta because it may be contaminated with Listeria monocytogenes, a bacteria that can cause serious infections. The recall affects products sold at Walmart with lot numbers L6079C or L6080C and expiration dates of 09/19/2027 or 09/20/2027. No illnesses have been reported so far.

Serious·FDA·Sep 15, 2026·Gias FoodsUpdated Oct 1

Sold nationwide. Centric Compounding has recalled six lots of Glutathione, Myer's Cocktail, and Tri-Immune Boost injectable vials due to elevated endotoxin contamination. The company has received nine reports of adverse reactions including fever, chills, chest pain, nausea, vomiting, headache, and malaise. Elevated endotoxins in injectable products can cause serious medical events including fever, low blood pressure, inflammatory reactions, anaphylactic shock, and death.

Serious·FDA·Sep 11, 2026·Centric Compounding

Sold nationwide. These six-drawer wood dressers can tip over and trap children if not anchored to the wall. The dressers do not meet federal safety standards required for furniture that children could access.

Serious·CPSC·Sep 10, 2026·FJTJBSI

Sold nationwide. The engine rocker arm on certain 2025 and 2026 Triumph TF450 competition motorcycles can seize or stick, causing the exhaust valves to remain open or break. This can lead to sudden loss of engine performance and increased risk of a crash. Triumph has received 12 reports of this problem, including one injury.

Serious·CPSC·Sep 10, 2026·Triumph

Sold nationwide. These finger light toys contain button cell batteries that children can easily access and swallow. Swallowed button batteries can cause serious internal injuries, chemical burns, and death.

Serious·CPSC·Sep 10, 2026·Cade

Sold nationwide. Certain dual fuel ranges manufactured between March 2025 and July 2026 may be missing a cap on the gas test port. This missing cap can allow gas to leak, creating a risk of fire or explosion. No injuries have been reported so far.

Serious·CPSC·Sep 10, 2026·AGA Rangemaster

Sold nationwide. Prepared Hero fire spray canisters can deteriorate over time and rupture, potentially failing to work during a fire. The company has received nine reports of canisters exploding or deteriorating while in storage. The affected canisters are marked with date code "09/2024" on the base.

Serious·CPSC·Sep 10, 2026·Prepared Hero

Sold nationwide. These hair dryer brushes lack a safety device that prevents electrocution if they fall into water while plugged in. They can also overheat and cause burns. One unit was reported to overheat and melt.

Serious·CPSC·Sep 10, 2026·Wantefully

Sold nationwide. The zipper on Lontcs Busy Board toys contains lead levels that exceed the federal lead paint safety standard. Lead is toxic if swallowed by young children and can cause serious health problems. The toys were sold online through Amazon from May 2024 to July 2026.

Serious·CPSC·Sep 10, 2026·SQT

Sold nationwide. Sweet Cubby children's loungewear sets do not meet federal flammability standards for sleepwear. The two-piece sets (short-sleeved shirt and shorts) sold online can catch fire more easily than safe sleepwear, posing a risk of serious burn injury. About 12,461 sets were sold through SHEIN.com between June 2025 and May 2026.

Serious·CPSC·Sep 10, 2026·Sweet Cubby

Sold nationwide. Junkins hair dryer brushes (model XR-8801) lack safety features that prevent electrocution if the device falls into water while plugged in. The product also poses a fire risk; there have been 10 reports of smoking or fire, though no injuries yet.

Serious·CPSC·Sep 10, 2026·Junkins

Sold nationwide. Victgoal-branded bicycle helmets do not meet mandatory safety standards for retention, stability, and certification. The helmets may fail to protect a rider's head in a crash, creating a serious risk of injury or death. Only red size-small helmets manufactured in November 2025 are affected.

Serious·CPSC·Sep 10, 2026·Keben

Sold nationwide. The rolling ball on Ricky Joy Sour Crush candy bottles can detach and become a choking hazard. These small plastic bottles with liquid sour candy were sold individually and in multi-packs in blue, red, green, and pink flavors at major retailers and online from January 2023 through May 2026.

Serious·CPSC·Sep 10, 2026·Ricky Joy

Sold nationwide. Cardinal Health is recalling 12 procedure kits that include BD Urinary Catheter Trays with CliniClean Pericare Wipes. The wipes may be contaminated with a lubricant used during manufacturing. If a contaminated wipe is used on a patient, it may cause localized skin irritation, redness, or mild inflammation. No injuries have been reported.

Moderate·FDA·Sep 9, 2026·Cardinal Health12 products