New York recalls

Red knobs on the Esjay Toddler Busy Board can detach, posing a choking risk for children under three. The toy violates federal small parts safety rules. No injuries have been reported, but the hazard is serious.

These 30-piece magnetic toy sets contain high-powered magnets in the hands and feet that can come loose and be swallowed by children. When multiple magnets are ingested, they can attract each other inside the digestive system, causing serious injuries including intestinal perforation, blockage, and blood poisoning. Two children have already been hospitalized after removing and swallowing magnets from these toys.

The grounding wire inside these electric grills can disconnect from the heating element, which removes a safety layer that normally protects against electric shock. This affects specific models made between October and December 2025. No injuries have been reported.

Windstone Medical Packaging's AMS Convenience Kit DSAEK Pack contains saline solution bags with blue connector pieces that may detach from the infusion port during normal use. This could allow contamination or improper fluid delivery during ophthalmic surgery.

Nipro Renal Solutions' Citric Complete Liquid Citric Acid Concentrate contains higher-than-safe levels of endotoxins, which are bacterial substances that can cause serious reactions in hemodialysis patients. The affected product was distributed across the US and internationally in specific lot numbers.

Nipro Renal Solutions USA is recalling specific lots of Citric Complete Dry Citric Acid Concentrate used in hemodialysis because they contain higher-than-safe levels of endotoxin, a bacterial substance. The affected product was distributed nationwide and internationally.

Nipro Renal Solutions USA is recalling specific lots of MedicaLyte Bicarbonate Powder used in hemodialysis treatment. The powder contains higher-than-safe levels of endotoxins, which are bacterial contaminants that can cause serious reactions in patients undergoing dialysis. The affected lots were distributed nationwide and internationally.

Nipro Renal Solutions USA recalled certain lots of MedicaLyte Liquid Bicarbonate Concentrate (models BC-100 and BC+201) used in hemodialysis because they contain elevated endotoxin levels. High endotoxin in dialysis concentrates can cause serious reactions during treatment.

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.

C.R. Bard has recalled multiple Bardex and SureStep Foley and intermittent catheter trays because the Pericare wipes included in these kits may have contamination on their surface. The contamination was identified through complaints received by the company.

Atrium Medical Corporation (Getinge) identified an Out of Specification result for bacterial endotoxin testing in specific lots of PVC Thoracic Catheters. Two lots—one 28FR model and one 36FR model—were affected. The contamination was found during quality testing.

Getinge PVC Thoracic Catheters in several sizes (24FR, 28FR, 32FR, and 36FR) failed bacterial endotoxin testing in specific lots. Endotoxins are substances from bacteria that can trigger immune reactions if present on medical devices.

Atrium Medical Corporation (Getinge) identified an out-of-specification result for bacterial endotoxin in specific lots of PVC thoracic catheters used in medical procedures. The affected catheters were distributed nationwide. No injuries have been reported to date.

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.

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.

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.

International Sprout Holdings' alfalfa product (50 lb. bags, Lot SAL2-24JB) has been recalled due to potential E. coli and Salmonella contamination. The affected product was distributed wholesale to food service operators and retailers across 16 U.S. states, Puerto Rico, Canada, Mexico, Tahiti, and Venezuela.

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).

Crown Farms Dried Suri Cut ribbon fish was not properly cleaned before drying, which can allow harmful bacteria to grow. The affected product was distributed in Virginia, New York, New Jersey, and Michigan.

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.

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.

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.

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.

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.

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.

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.

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.

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.

A&P Creations LLC is recalling X10 Natural Enhancement Supplement because it contains sildenafil and tadalafil—active ingredients in prescription drugs Viagra and Cialis—that are not listed on the label. These hidden ingredients can dangerously lower blood pressure, especially when combined with nitrate medications used for heart conditions.

A&P Creations LLC is recalling biQ-FEL, a dietary supplement sold in 500 mL bottles, because it contains undeclared sildenafil and tadalafil—the active ingredients in prescription erectile dysfunction drugs Viagra and Cialis. These hidden ingredients can dangerously lower blood pressure if combined with certain heart medications like nitroglycerin.