Iowa recalls

Sold nationwide. Becton Dickinson has recalled certain ForeSight Elite tissue oximetry cables due to incorrect labeling of Channel 1 and Channel 2 on the module and flag labels. This labeling error could cause clinicians to misread oxygen saturation data if the cables are connected to the wrong channels. The affected cables were distributed to hospitals and healthcare facilities.

Moderate·FDA·Sep 30, 2026·Becton Dickinson

Sold nationwide. A software issue in Philips EPIQ Elite ultrasound systems (Model 795234, software version 14.0) causes doppler blood flow measurements to display at incorrect depths. This can lead to inaccurate velocity readings and potential misdiagnosis of vascular conditions. About 219 units are affected worldwide.

Moderate·FDA·Sep 30, 2026·Philips

Sold nationwide. A small number of Pearle Vision 1 day contact lenses in one affected lot were manufactured with incorrect lens power. This could result in blurred or distorted vision if the wrong lens is worn. No injuries have been reported.

Moderate·FDA·Sep 30, 2026·CooperVision

Sold nationwide. Olympus is recalling four BiCOAG Hemostasis Probe models because they may have been made without the full amount of adhesive, so the ceramic tip could detach. The recall covers 3,467 units sold in the US and several other countries. No injuries have been reported.

Moderate·FDA·Sep 30, 2026·Olympus4 products

Sold nationwide. Philips is recalling 12 groups of MRI systems and related upgrade products because of a software issue. If scan settings are manually adjusted so the image processing needs more memory than the system has, the examination can end partway through. No injuries have been reported.

Moderate·FDA·Sep 30, 2026·Philips12 products

Sold nationwide. Some units of the Biomerieux VITEK 2 AST-N461 test kit used to determine antibiotic susceptibility in gram-negative bacteria have damaged card pouches. This damage can cause the test to report false resistant results, which may lead to use of less effective antibiotics or unnecessary antibiotic combinations.

Moderate·FDA·Sep 30, 2026·bioMérieux

Sold nationwide. Medline convenience kits (models DYNJ48258D and DYNJ48258F) contain Healthmark Instrument Channel Brushes with a potential sharp edge or burr on the brush end. This sharp edge could cause a cut, abrasion, or infection if the brush is handled or used.

Moderate·FDA·Sep 30, 2026·Medline2 products

Sold nationwide. SeaSpine Orthopedics is recalling certain Extended Polyaxial Head spinal implants (model MD1-300010-12) because the proximal thread depth does not meet design specifications. This defect could affect the secure attachment of the device during spinal surgery. No injuries have been reported.

Moderate·FDA·Sep 30, 2026·SeaSpine

Sold nationwide. Fresenius Medical Care is issuing a communication regarding its CombiSet hemodialysis blood tubing set (Model 03-2522-1) to ensure healthcare providers and patients review the product's instructions for use. The company is recommending that all treatment preparation and handling steps be performed exactly as instructed to maintain safe operation.

Moderate·FDA·Sep 30, 2026·Fresenius Medical Care

Sold nationwide. Maquet PowerLED 300 concealed lighting systems may detach at the connection between the spring arm and suspension arm. This could cause the device to fall and potentially injure someone in an operating room or clinical setting.

Moderate·FDA·Sep 30, 2026·Maquet

Sold nationwide. Ventec Life Systems is recalling three HomeFill oxygen cylinder products, 48 units in total. The cylinders do not have the medical gas labeling required by regulators. No injuries have been reported. The recall covers units distributed in Florida, Iowa, Ohio, Nebraska, and Tennessee.

Moderate·FDA·Sep 30, 2026·Ventec Life Systems3 products

Sold nationwide. 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.

Moderate·FDA·Sep 30, 2026·Midmark4 products

Sold nationwide. 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.

Moderate·FDA·Sep 30, 2026·Olympus

Sold nationwide. 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.

Moderate·FDA·Sep 30, 2026·Heidelberg Engineering

Sold nationwide. 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.

Serious·FDA·Sep 30, 2026·Boston Scientific

Sold nationwide. CooperSurgical is recalling two INCA infant nasal CPAP product lines, 2,792 boxes (13,960 units) in total, because the flexible tubing may loosen from the nasal cannula during assembly or use. A loose connection can cause a loss of CPAP pressure, which may reduce treatment effectiveness and lower oxygen levels until the connection is restored. No injuries have been reported.

Serious·FDA·Sep 30, 2026·CooperSurgical2 products

Sold nationwide. 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.

Serious·FDA·Sep 30, 2026·bettergoods

Sold nationwide. 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.

Moderate·FDA·Sep 30, 2026·So Delicious Dairy Free

United Sugar Producers & Refiners is recalling two 50-pound sugar products because they may contain wheat kernels. The products are light brown sugar (item 810051) and United 6X powdered sugar (item 810087), sold under the United name and at least one other brand. The products were distributed in IA, IL, IN, KS, MN, OH, PA, and TX. No injuries have been reported.

Moderate·FDA·Sep 30, 2026·Good & Gather2 products

Sold nationwide. Prestige Consumer Healthcare is recalling 2 products, both Clear Eyes Redness Relief lubricant and redness reliever eye drops in 0.5 fl oz (15 mL) bottles, one sold with a hang tag. The company cannot assure the drops are sterile. No injuries have been reported, and about 2.4 million bottles were affected.

Moderate·FDA·Sep 30, 2026·Prestige Consumer Healthcare2 products

Sold nationwide. 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.

Moderate·FDA·Sep 30, 2026·Amneal Pharmaceuticals

Sold nationwide. 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.

Moderate·FDA·Sep 30, 2026·MacLeods Pharma

Sold nationwide. The FDA has announced a nationwide recall of 9 lubricant eye drops and one eye ointment sold under the Walgreens, AvKare, Reliable-1 Laboratories, TRP Gentle Eyes, Major LubriFresh P.M. and Cameron Pharmaceuticals names. The manufacturer could not confirm that the products are sterile, which is required for eye products. No injuries have been reported.

Moderate·FDA·Sep 30, 2026·Sterling Pharmaceutical Services9 products

Sold nationwide. 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.

Serious·FDA·Sep 30, 2026·ICU Medical

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.

FDA·Sep 30, 2026·Almond Joy

Sold nationwide. 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.

Moderate·FDA·Sep 26, 2026·Mezzetta

Sold nationwide. 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.

Serious·CPSC·Sep 24, 2026·ABC Trading

Sold nationwide. Love To Dream portable sleep machines contain a lithium-ion battery that can overheat if an incompatible charger is used. This overheating poses a risk of fire or burns.

Moderate·CPSC·Sep 24, 2026·Love To Dream

Sold nationwide. The left temple of INMO Air3 Smart Glasses can overheat during extended use, causing burns to the face and ear. The company has received 10 reports of overheating, including burning sensations. The affected glasses were sold online between December 2025 and August 2026.

Serious·CPSC·Sep 24, 2026·INMO

Sold nationwide. Style Homeware Emerspring mattresses sold on Amazon do not meet federal flammability standards for mattresses. This poses a risk of serious injury or death if a fire occurs near the mattress.

Serious·CPSC·Sep 24, 2026·Style Homeware