New York recalls

American Regent's aminocaproic acid injection (250 mg/mL) has been recalled because batches contain particulate matter including hair, glass, and/or paraformaldehyde. The contamination affects 20 mL vials distributed nationwide. This is a prescription medication used to control bleeding.

American Regent's cyanocobalamin (vitamin B12) injection has been recalled due to contamination with particulate matter, including hair, glass, and/or paraformaldehyde. The affected product is a 10,000 mcg/10 mL multi-dose vial (Lot #25082, expiring 3/31/2027). This is a prescription medication administered by injection.

American Regent's Cyanocobalamin injection (vitamin B12) has been found to contain particulate matter, including hair, glass, and paraformaldehyde. The contamination affects specific lot numbers distributed nationwide. This is a prescription medication given by injection.

American Regent's nitroglycerin injection (50 mg/10 mL vials) has been found to contain particulate matter, including hair, glass, and/or paraformaldehyde. This affects lot #24291 with an expiration date of 8/31/2026, distributed nationwide. The contamination was discovered during quality testing.

Some Fresenius Kabi morphine sulfate prefilled syringes are labeled as morphine 2 mg/mL but actually contain Dilaudid (hydromorphone) 0.5 mg/0.5 mL. This labeling error could lead to patients receiving the wrong medication and dose. The affected lot is 6402820 with an expiration date of 12/2028.

Mylan Pharmaceuticals is recalling one lot of Acamprosate Calcium 333 mg delayed-release tablets because they failed to meet dissolution specifications—meaning the tablets may not break down and release the medication as intended in the body. This could result in ineffective treatment. No injuries have been reported.

Golden State Medical Supply is recalling Carbamazepine Tablets, USP 200mg due to black specks found in some tablets. This is a manufacturing quality issue. The affected lots were distributed nationwide.

Sun Pharmaceutical's Carbamazepine 200mg tablets (Lot #AD94033, expiring 5/31/2028) contain black spots caused by burnt ingredients during manufacturing. The tablets do not meet quality standards, though no injuries have been reported.

Regeneron is recalling one lot of Libtayo (cemiplimab-rwlc), an intravenous cancer treatment, because the manufacturer cannot guarantee the vials are sterile. This affects lot 8494000002, which expires July 31, 2028. About 21,353 vials are involved in the recall nationwide.

Certain vials of PEMRYDI RTU (pemetrexed injection) have shown green to dark green discoloration. The manufacturer received complaints from the field about affected vials. The discoloration may indicate a quality or sterility concern.

Certain vials of PEMRYDI RTU (pemetrexed injection) have developed green to dark green discoloration. The affected lots are P400172 and PA00050A, expiring 09/30/2027. Discoloration may indicate a quality issue with the medication.

The Better Bakehouse Snack Company recalled certain lots of Donutful Chocolate Dipped Vanilla Cake Donuts because they may contain milk that is not listed on the label. People with a milk allergy or severe sensitivity could have a serious allergic reaction if they eat this product.

Baxter is recalling two lots of 0.9% Sodium Chloride Injection (saline solution) used in hospitals and dialysis centers because fiberglass particles have been found in the solution. The affected lots were distributed to hospitals and medical suppliers in 14 states between July 31 and August 3, 2026. No injuries have been reported so far.

Baxter is recalling one lot of 70% Dextrose Injection used in hospitals and care facilities because stainless steel particles were found in the solution. If given intravenously, these particles could cause blood clots, block blood vessels, or damage organs. No patient injuries have been reported so far.

Vitruvias Therapeutics is recalling one lot (504950) of Thyroid Tablets, USP 30 mg because testing found the tablets may contain higher-than-intended amounts of thyroid hormone. Taking overly potent thyroid medication can cause an overactive thyroid, leading to weight loss, rapid heartbeat, chest pain, and other serious symptoms, especially in elderly people, pregnant women, and infants.

Fromm Family Foods is recalling two wet dog food products: Turkey Pâté and Diner Classics Milo's Meatloaf Pâté, sold in 12.2 oz. and 12.5 oz. cans with a Best By date of 032029. The recall is due to potential metal contamination discovered during production. If dogs eat metal, they can choke, vomit, lose appetite, or suffer cuts and blockages in the mouth or digestive tract.

CCM Hockey visors and replacement visor accessories can crack when hit during play, potentially causing cuts or impact injuries. The recalled products are FMHVR Hybrid Visors and ACCHVR Replacement Visor accessories with specific serial numbers.

Workbless pressure washer models WB0301 and WB0302 lack proper electrical safety features—specifically a ground-fault circuit-interrupter (GFCI) and an adequate power cord. This creates a serious risk of electric shock or electrocution during use.

Koorlian brand mattresses sold on Amazon do not meet federal flammability safety standards and pose a serious fire risk. The recalled mattresses are 10 inches thick, Twin XL size, with white tops and blue sides, and were sold compressed in boxes between November 2025 and March 2026.

These small LED tea lights contain button-cell batteries that children can easily access and swallow. Swallowed button batteries can cause serious internal injuries, chemical burns, and death. The product also lacks required safety warnings.

The circuit board in Goal Zero's YETI 3000X power stations can overheat, which may cause the unit to catch fire or smoke. Goal Zero has received four reports of units catching fire or overheating, though no injuries have been reported so far.

The ventilation fan motor in Modine's Airedale heating and cooling units can short circuit if water reaches the circuit board, causing the units to overheat and potentially catch fire. The affected models are ClassMate and SchoolMate heat pumps installed in schools and classrooms since 2013. Modine has received 11 reports of fires causing over $2.7 million in property damage.

The rear brake caliper on certain 2021–2024 Husqvarna and GASGAS off-road motorcycles can crack or break, which reduces braking power and increases the risk of a crash. About 21,040 motorcycles are affected. No injuries have been reported so far.

Optimal Balance Pharmacy identified elevated bacterial endotoxin levels in one lot of compounded glutathione 200 mg/mL multi-dose vials during testing. Endotoxins can cause fevers, low blood pressure, severe allergic reactions, and in serious cases, death. The pharmacy has already received reports of adverse events including fever, chills, severe headache, nausea, vomiting, and allergic-like reactions.

B. Braun Medical Inc. is recalling one lot of Excel Lactated Ringers Injection (1000mL) distributed to hospitals and healthcare facilities because the solution contains small particles—primarily cellulose fibers from cotton, wood, and polystyrene. These particles could cause blood clots, vein inflammation, or organ damage if infused intravenously. No injuries have been reported so far.

529 Commerce's aquafaba powder (vegan egg replacement) contains undeclared egg, which is a serious allergen risk. The product was distributed across 22 states. People with egg allergies who consume this powder could have an allergic reaction.

Baxter Healthcare Corporation is recalling one lot of Cefazolin in Dextrose injection due to the presence of particulate matter in the solution. The affected product is a frozen premix infusion bag used for intravenous antibiotic treatment. This is a Class I recall, the most serious classification.

Liebel-Flarsheim Company LLC is recalling Optiray Imaging Bulk Package-350 (ioversol injection 74%, 350 mg/mL) due to the presence of particulate matter—including plastic, stainless steel, and glass—found in affected vials. The contamination affects lot #25ZF3670 with an expiration date of May 31, 2027, distributed nationwide in the US and Mexico.

Victory Medical Center Pharmacy's Glutathione injectable solution (200 mg/mL) failed sterility testing and was found to contain elevated bacterial endotoxin levels, which are out of acceptable limits. The affected product was distributed nationwide in specific lots with expiration dates through August 2026.

Buy-Herbal's Kian Pee Wan Capsules contain two prescription drug ingredients—dexamethasone and cyproheptadine—that are not listed on the label and were not approved by the FDA. The product was sold online through eBay. No injuries have been reported.