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Henry Schein is recalling two dental restorative products, Structur 2 SC Temporary Resin Cartridge Refill and Grandio Universal Nano-Hybrid Restorative Material Capsules, with 974 units affected. Specific lots were distributed in the U.S. and Barbados with incorrect packaging and Instructions for Use from the FDA-cleared device.

Moderate·FDA·Sep 2, 2026·Henry Schein2 products

Fixing screws on the ceiling movement gear of the suspended arm in Canon Medical Alphenix interventional X-ray systems may become loose over time. This could potentially cause the arm to shift during use. Ten systems are affected across eight U.S. states.

Moderate·FDA·Sep 2, 2026

Midmark is recalling two digital electrocardiogram (ECG) products, including the IQecg Digital ECG and the Digital ECG HD+12 and HD+15, because a communication anomaly may cause incorrect heart waveforms and an inaccurate beats-per-minute reading. The recall covers software versions of the IQecg Plugin starting with v10 and before v10.1.0.18. No injuries have been reported.

Moderate·FDA·Sep 2, 2026·Midmark2 products

AVID Medical is recalling seven Halyard medical kit products because the labeling does not disclose that the StatLock component contains natural rubber latex. The kits were distributed nationwide, including in Mississippi and Texas. No injuries have been reported.

Moderate·FDA·Sep 2, 20267 products

Merge Healthcare's PACS and OrthoPACS medical imaging workstations contain a software issue that may cause measurements to be displayed inaccurately. Version 9.5 is affected. The issue was identified in 20 units distributed across California, Florida, Kentucky, Nebraska, and Washington.

Moderate·FDA·Sep 2, 2026·Merge Healthcare

American Contract Systems is recalling 4 convenience kit models that contain Medline Red Rubber Intermittent Catheters. Medline found that representative samples did not meet applicable performance specifications. The kits were distributed in Iowa and Ohio, and no injuries have been reported.

Moderate·FDA·Sep 2, 20264 products

Medline Industries distributed 45 tracheostomy tube kits (SKU DYKM2330) with incorrect component labeling. The discrepancy between the kit label and its contents could lead to confusion during use. No injuries have been reported.

Moderate·FDA·Sep 2, 2026

Hollister has identified a manufacturing defect in select lots of Onli Hydrophilic Urethral Intermittent Catheters that may cause a protrusion on the catheter tip. This defect could lead to genitourinary trauma or bleeding during use.

Moderate·FDA·Sep 2, 2026·Hollister

Medline is recalling specific lots of its medical convenience kits that contain Pilling Wecksorb Neurosponges and Neurosponge Strips. The neurosponges may have endotoxin levels above specification. The recall covers four product groups, about 6,950 kits in total, distributed in several US states. No injuries have been reported.

Moderate·FDA·Sep 2, 20264 products

Medline is recalling three neonatal and infant heated wire breathing circuit products, about 417,000 units in total. The heated wire connector at the humidifier can fail and show discoloration, melting, smoke, or a burning odor. Failure could cause breathing problems in infants, and no injuries have been reported.

Serious·FDA·Sep 2, 20263 products

Philips Incisive CT scanners running software versions V4.5 or V5.0 may fail to start a clinical scan during Bolus Tracking imaging procedures. This could delay or prevent necessary diagnostic scans from being acquired.

Moderate·FDA·Sep 2, 2026

Africando Foods LLC's Alfredo Hot Sauce is missing wheat and soybean oil from its ingredient label. Wheat is present as a sub-ingredient in the chicken bouillon, and soybean oil was used but not listed. The affected product was distributed to wholesale and retail locations in Iowa, Kentucky, and Illinois.

Moderate·FDA·Sep 2, 2026

Horizon Organic 1% chocolate milk in 8 oz cartons (sold in 12-count and 18-count multipacks) may be spoiled. The affected products have best-by dates between January 28 and February 3, 2027, and were distributed across the United States.

Moderate·FDA·Sep 2, 2026·Horizon Organic

Upstate Niagara Cooperative's Mehadrin Chocolate Leben 6 oz cups may not have been properly pasteurized, which could allow harmful bacteria to survive. The affected product was distributed in New Jersey and has a use-by date of 10/14/26.

Moderate·FDA·Sep 2, 2026·Mehadrin

Jaime's Foods ATX Jalapeno Ranch dressing in 16 oz. glass jars may contain egg, which is not declared on the label. People with egg allergies could have a serious reaction if they consume this product. The recall affects 102 cases distributed in Texas.

Serious·FDA·Sep 2, 2026

Byron White Formulas is recalling three herbal supplements sold as A-L Complex, A-P, and A-FNG, all in 1.0 fl. oz. (30 mL) bottles. The English labels do not list walnuts, which are in the product, so people with a walnut allergy may not know it is there. No injuries have been reported.

Moderate·FDA·Sep 2, 20263 products

Lidl is recalling two Eridanous Greek Style shortbread cookie products, 330 g each, because some packages have labels only in foreign languages. The cookies contain wheat, soy, milk, eggs and coconut, which are not listed in English on the label. The products were shipped to stores in DC, DE, GA, MD, NJ, NY, NC, PA, SC and VA.

Moderate·FDA·Sep 2, 20262 products

bettergoods brand Pistachio Nut Butter (6.7 oz jars) may be contaminated with Salmonella. The affected product has lot number LB028ACP04 with an expiration date of January 28, 2027, and was distributed across 19 states.

Serious·FDA·Sep 2, 2026

Marketside Tomato Bisque Soup Kit tested positive for Listeria monocytogenes, a bacteria that can cause serious illness. The affected product is a 14 oz ready-to-heat soup kit with UPC 1 94346474004 and a Best By date of 8/22/2026.

Moderate·FDA·Sep 2, 2026

Dreyer's is recalling six Outshine fruit bar products because they may contain pieces of glass. The recall covers Strawberry, Watermelon, Grape, Tangerine and Black Cherry 6-count packs, plus a 24-count variety pack of Strawberry, Pineapple, Grape and Tangerine bars. No injuries have been reported.

Serious·FDA·Sep 2, 2026·Outshine6 products

ZMB Enterprises' Addall XR Shot 1 liquid dietary supplement contains three undeclared ingredients that are banned or restricted by the FDA: 1,4-DMAA, Phenylethylamine, and Phenibut. The product was sold online between July and December 2025.

Serious·FDA·Sep 2, 2026

Sirna & Sons Produce has recalled 1-pound bags of jalapeño peppers that may be contaminated with Salmonella Javiana. The affected product was packed on July 13 or July 23, 2026, and distributed to food service locations in Ohio and Pennsylvania.

Serious·FDA·Sep 2, 2026

Khong Guan is recalling two sizes of its glutinous rice balls with black sesame filling, 14.1 oz (400 g) each, because they may contain peanuts that are not listed on the label. The recall covers two UPC products, both made in China and sold in AZ, CA, CO, HI, NJ, OR, TX and WA. No illnesses have been reported.

Serious·FDA·Sep 2, 20262 products

Sun Noodle's Sura Tanmen Hot and Sour Flavor ramen noodle kit contains a soba sauce packet with fish (bonito, sardine, and mackerel), but the package label does not disclose these fish allergens. This poses a risk to people with fish allergies. About 140 packages were distributed in Hawaii.

Serious·FDA·Sep 2, 2026·Sura

B. Braun Medical has recalled Lactated Ringer's Injection USP in 1000 mL EXCEL containers due to the presence of particulate matter. The affected lot is J4H077 with an expiration date of November 30, 2026. About 23,688 bags were distributed nationwide.

Serious·FDA·Sep 2, 2026

Hikma Pharmaceuticals is recalling specific lots of Ramipril Capsules 10 mg because testing found higher-than-allowed levels of dicyclohexylurea, a process impurity. The affected lots are AC5470A and AC5470B, both expiring July 2027. No injuries have been reported.

Moderate·FDA·Sep 2, 2026·Hikma Pharmaceuticals

Fresenius Kabi USA discovered that Tyenne (tocilizumab-aazg) Injection vials may contain glass particles. The contamination was found during an internal investigation. The affected lot is 16UI07, which expires August 31, 2028.

Serious·FDA·Sep 2, 2026

Apotex Corp. is recalling one lot of Paxil CR (paroxetine) 37.5mg extended-release tablets because the medication failed to meet dissolution specifications during 24-month stability testing. This means the tablets may not release the drug into the body as intended. The affected lot (TY9494, expiration 05/31/2027) was distributed nationwide.

Moderate·FDA·Sep 2, 2026

Mallinckrodt has recalled specific lots of Acthar Gel (repository corticotropin injection) due to the presence of glass and stopper pieces in the vials. This contamination could pose a risk if the affected medication is used. The recall affects 12,367 vials with lot numbers 1564-107 and 1564-107H, both expiring January 31, 2027.

Moderate·FDA·Sep 2, 2026·Mallinckrodt

FDA inspection found that Zicam Cold Remedy Medicated Nasal Swabs failed microbiological testing, meaning they may contain harmful microbes. The affected products were manufactured under conditions that did not meet federal safety standards. Specific lot numbers with expiration dates through August 2028 are involved.

Moderate·FDA·Sep 2, 2026·Arm & Hammer