New York recalls

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.

Heritage Pharmaceuticals' clindamycin palmitate hydrochloride oral solution (75 mg/5 mL) has been recalled due to the presence of particles and white flakes found in reconstituted bottles. The affected lot is 2411550, which expires November 2026. This product was distributed nationwide.

CLEAR EYES Maximum Itchy Eye Relief eye drops may not be sterile due to potential contamination. The affected product is the 0.5 fl oz (15 mL) dropper bottle, Lot 2552A with expiration date 09/30/2027. No injuries have been reported.

The FDA identified Current Good Manufacturing Practice (CGMP) deviations during an inspection of Shoolin Pharma Chem LLP, a supplier of sildenafil citrate USP—an active pharmaceutical ingredient used in prescription compounding. One lot (SDC2505001) distributed nationwide has been recalled due to these manufacturing control issues.

The FDA identified manufacturing practice violations (CGMP deviations) during an inspection of Shoolin Pharma Chem's facility in India. One batch of tadalafil USP powder used for prescription compounding was distributed nationwide in the USA and does not meet required manufacturing standards.

The FDA identified current good manufacturing practice (CGMP) deviations during an inspection of Shoolin Pharma Chem LLP's facility in India. The company manufactures tadalafil USP powder (active pharmaceutical ingredient) intended for prescription compounding use. One batch (TLF2506001, expiring May 31, 2028) totaling 20 kg was distributed nationwide in the USA.

Shoolin Pharma Chem LLP's tadalafil USP powder (lot TLF2506001) was found to have deviations from good manufacturing practices during an FDA inspection. The affected product is a 100-gram bag intended for prescription compounding only.

The FDA identified Current Good Manufacturing Practice (CGMP) deviations during an inspection of Shoolin Pharma Chem LLP's facility in India. Sildenafil citrate bulk powder (batch SDC2505001, expiring April 30, 2030) distributed nationwide for prescription compounding did not meet required manufacturing standards.

Apollo Care's semaglutide 20mg injection vials contain visible particles made of nylon/polyamide and silk-like material. The particles were found during quality testing. The affected vials were distributed nationwide.

Apollo Care's semaglutide 10mg injection vials contain visible particles made of nylon, polyamide, and silk-like material. The contamination was identified in lot AC-017274 (expiration 12/12/2026), affecting 500 vials distributed nationwide. No injuries have been reported.

Apollo Care is recalling one lot of semaglutide 7.5mg injection vials due to the presence of particulate matter (nylon/polyamide and silk-type material) in the medication. The contamination was identified during quality testing. No injuries have been reported to date.

Apollo Care's semaglutide 5mg injection vials contain particulate matter identified as nylon/polyamide and silk/proteinaceous material. This contamination affects one lot (AC-017272, expiring 12/12/2026) of approximately 250 vials distributed nationwide. No injuries have been reported.

Apollo Care is recalling one lot of semaglutide injection due to the presence of visible particles identified as nylon/polyamide and silk material in the vials. The contamination was discovered in lot AC-017271 (expiration 12/12/2026). No injuries have been reported.