New York recalls

Midmark Corporation's IQvitals Zone vital signs monitor may produce inaccurate blood pressure readings when using the Linear Deflation Method. The device measures blood pressure, pulse, temperature, and oxygen levels for adult and pediatric patients. A limited number of units with specific serial numbers are affected.

Midmark Corporation's IQvitals Zone vital signs monitor may display inaccurate blood pressure readings when using the Linear Deflation Method. This affects Model 1-200-0320 with Kit 4-000-0622. The device measures blood pressure, pulse, temperature, and oxygen saturation for adult and pediatric patients.

Some Olympus EZDilate Endoscopic Balloon Dilator devices (Model BD-420X-1355) have an incorrect label on the shaft. The inflation chart label may show balloon sizes of 18, 19, or 20 mm when the actual device is 11, 12, or 13 mm. This mislabeling could lead to confusion during use.

The wheels on Heidelberg Engineering's SPECTRALIS imaging device may come loose when the module is pushed or pulled during movement or transportation. If wheels loosen, the stand can become unstable and tip over, potentially causing impact or crushing injuries to nearby people.

The tip of certain Boston Scientific Imager II Angiographic Catheters may fracture or detach during use. Fragments could remain in the patient's body or travel through blood vessels, potentially causing a prolonged procedure or life-threatening blood clot.

CooperSurgical's INCA neonatal nasal CPAP replacement tubing sets may develop a loose connection between the flexible tubing and nasal cannula during assembly or use. A loose connection can cause loss of CPAP pressure, potentially reducing treatment effectiveness and oxygen delivery to the infant until the connection is restored.

CooperSurgical's INCA infant nasal CPAP devices may develop a loose connection between the flexible tubing and nasal cannula during assembly or use. This loose connection could cause a loss of CPAP pressure, reducing treatment effectiveness and potentially lowering oxygen levels until the connection is restored.

bettergoods Lemon Alfredo Fettuccine pasta distributed by Walmart may be contaminated with Listeria monocytogenes, a harmful bacteria. The affected product was made in Italy and sold nationwide at Walmart locations. No illnesses have been reported so far.

Whole Foods Market is recalling Fromagerie Coop de Mean Cabricharme and Belgium Cabricharme cheese sold in slices because they contain egg that is not declared on the label. People with egg allergies could have a serious reaction if they eat this cheese.

So Delicious Dairy Free Salted Caramel Cluster Cashewmilk (16 oz tubs) may contain small stones or other hard objects. The product was distributed nationwide. No injuries have been reported.

Clear Eyes Redness Relief eye drops may not be sterile due to a manufacturing issue. The affected lots are RL25G04 (expires 07/2027) and RL2H02 (expires 08/2027). No injuries have been reported.

Clear Eyes Redness Relief eye drops distributed nationwide may not meet sterility standards required for products applied directly to the eye. The FDA has recalled specific lot numbers manufactured between July and November 2027. No injuries have been reported, but eye drops that are not sterile can pose a risk of infection.

Some prefilled pens of Amneal Exenatide Injection may contain no medication due to a defective delivery system. This affects lot AP250095A (expiration 2/28/2027). Patients relying on these pens may not receive their intended dose.

Macleods Pharmaceuticals has recalled Olanzapine Tablets USP 5 mg (lot BOB22321A, expiring 07-31-2027) because testing found organic impurities above acceptable limits. The affected bottles were distributed nationwide. No injuries have been reported.

AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% lubricant eye drops in 2-count twin packs may not meet sterility standards. The affected lots were distributed nationwide. Use of non-sterile eye drops could increase the risk of eye infection.

Cameron Pharmaceuticals lubricant eye drops (carboxymethylcellulose sodium 0.5%) in 15 mL bottles may not meet sterility standards. The affected products are Lot #3163 (expiry 8/31/2026) and Lot #3164 (expiry 9/30/2026). About 19,284 bottles were distributed nationwide.

Major Pharmaceuticals is recalling LubriFresh P.M. Nighttime Ointment (0.125 oz tubes, Lot #3183) because the manufacturer cannot confirm the product meets sterility standards. This means the product may not be free from unwanted microorganisms.

TRP The Relief Products Gentle Eyes Lubricant Eye Drops may not be sterile due to a manufacturing issue. Two specific lots are affected: Lot #3279 (expires 6/30/2027) and Lot #3292 (expires 5/31/2027). Approximately 14,538 bottles were distributed nationwide.

Reliable-1 Laboratories Lubricating Tears eye drops may not be sterile due to manufacturing or quality control issues. The FDA is recalling specific lots distributed nationwide to ensure patient safety.

Walgreens Lubricant Eye Drops in 2-count twin packs may not be sterile due to a manufacturing issue. The affected lots were distributed nationwide. No injuries have been reported, but eye drops must be sterile to be safe for use.

Walgreens Lubricant Eye Drops (carboxymethylcellulose sodium 0.5%) in 0.5 oz bottles may not be sterile. The product is meant to be sterile for safe use in the eye. Multiple lots distributed nationwide are affected.

Reliable-1 Laboratories is recalling Sodium Chloride Hypertonicity Ophthalmic Solution 5% (0.5 FL OZ bottles) because the manufacturer cannot assure the product was manufactured under sterile conditions. The affected lots are #3192 (expires 01/31/2027), #3293 (expires 06/30/2027), and #3336 (expires 06/30/2027). No injuries have been reported.

AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% lubricant eye drops failed to meet sterility standards. The product was distributed nationwide in 15 mL bottles across nine affected lot numbers with expiration dates ranging from August 2026 to July 2027. Use of non-sterile eye drops can introduce bacteria or other microorganisms into the eye.

ICU Medical's 0.9% Sodium Chloride Injection (100 mL) may be mislabeled. Some bags marked as sodium chloride may actually contain potassium chloride instead. This mix-up affects lot 1042188, expiring 10/31/2027, distributed nationwide.

Unilever's Almond Joy Ice Cream Bars (2.0 fl. oz.) have inaccurate Nutrition Facts information printed on the packaging. The affected products are 6-bar cartons distributed across the United States. No injuries have been reported.

Sierra Nevada Cheese Company is recalling all Graziers Raw Milk Cheese products (Monterey Jack, Jalapeño Jack, Medium Cheddar, and Sharp Cheddar) due to potential contamination with E. coli O26:H11, a dangerous strain that produces Shiga toxin. The FDA and CDC are investigating a multistate outbreak linked to these cheeses, with 13 illnesses identified so far.

A specific lot of Mezzetta Golden Greek Peperoncini Medium Heat (32 oz.) may contain a pest contaminant in the jar. The company identified the issue after a consumer video circulated on social media and immediately launched a voluntary recall of the affected lot. No illnesses or injuries have been reported.

Sempio Food Services Inc. recalled approximately 4,596 pounds of ready-to-eat chicken stew products imported from South Korea because they were not properly re-inspected upon entry into the United States. The products were produced on March 30, 2026, and have a best-by date of September 29, 2027. No illnesses or injuries have been reported.

Lior Cinnamon Ground Seasoning has been found to contain elevated levels of lead. The product was distributed to stores in New York, New Jersey, Pennsylvania, Texas, Florida, and Illinois between November 2025 and September 2026. No illnesses have been reported.

ABC Trading's light-up toys (ties, headbands, and glasses) contain button cell batteries in compartments that children can easily open. Swallowing these batteries can cause serious internal injuries, chemical burns, and death.