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Man Fon is recalling two wonton wrapper products: Man Fon Extra Thin Won Ton Wrappers in 10 oz packages, and wonton wrappers sold in clear plastic bags, including 16 oz bags and 4-lb bags labeled "Wonton Noodles." The products contain Yellow #5 and Yellow #6 food dyes that are not listed on the label. The product went mainly to California restaurants, with some sent to New Mexico grocery stores.

Moderate·FDA·Jul 29, 20262 products

Brooklyn Roasting Company's Pasteurized Cold Brew Concentrate (2.5-gallon bags) distributed April through June 2026 may develop botulism toxin if stored at room temperature. The product was pasteurized but may not be safe if kept outside refrigeration.

Moderate·FDA·Jul 29, 2026·Brooklyn Roasting Company

Vintage Roots Root Beer Syrup contains sassafras bark, an ingredient that is not approved for use in food by the FDA. The affected product is an 8 oz glass bottle with lot code 051626-1 and a use-by date of May 2027, distributed only in Montana.

Moderate·FDA·Jul 29, 2026·Vintage Roots

Fresenius Kabi is recalling five injectable medicine products because hair was found in some vials. The products are Xylocaine (two sizes), Naropin, lidocaine HCl injection and glycopyrrolate injection, all made by Fresenius Kabi in Lake Zurich, Illinois, and sold nationwide. No injuries have been reported.

Moderate·FDA·Jul 29, 20265 products

Rising Pharma's Cyproheptadine Hydrochloride Syrup (2 mg/5 mL, 473 mL bottles) is being recalled because the medication is crystallizing and forming particles that float in the bottle. This affects specific batches distributed nationwide. No injuries have been reported.

Moderate·FDA·Jul 29, 2026·Rising Pharma

Rohto-Mentholatum is recalling eight Rohto Cooling Eye Drops products because they lack assurance of sterility, meaning the drops may not be guaranteed free of microbial contamination. All eight are sold under the Rohto Cooling Eye Drops name: ALL-IN-ONE, Max Strength (three versions), Optic Glow, Digi Eye, Dry Aid (single and twin pack), and Cool Relief. No injuries have been reported.

Moderate·FDA·Jul 29, 2026·Rohto-Mentholatum8 products

Ascend Laboratories is recalling one lot of amlodipine and olmesartan medoxomil combination tablets (10 mg/20 mg) because the olmesartan medoxomil active ingredient is below the required amount. This means affected tablets may not work as intended to lower blood pressure.

Moderate·FDA·Jul 29, 2026

Major Pharmaceuticals is recalling one lot of Levothyroxine Sodium Tablets, USP, 25 mcg due to subpotency — meaning the tablets contain less active ingredient than labeled. This affects Lot N02212 with an expiration date of 07/2026. Patients taking subpotent levothyroxine may not receive the full intended dose of this thyroid hormone replacement medication.

Moderate·FDA·Jul 29, 2026·Major Pharmaceuticals12 products

Precision Dose Inc. is recalling one lot of Glycopyrrolate Oral Solution (1 mg/5 mL) due to an unidentified impurity found during routine stability testing that does not meet specification. The affected lot (506033) expires November 30, 2026. This medication is prescription-only and supplied in unit-dose oral syringes.

Moderate·FDA·Jul 29, 2026·Precision Dose

Rooted in Rare brand Aquafaba Powder may contain undeclared egg, posing a serious allergic reaction risk for people with egg allergies or sensitivities. The recall affects 4 oz and 12 oz packages distributed through Amazon and the company website between June 2025 and July 2026.

Moderate·FDA·Jul 29, 2026

Certain replacement side curtain air bag assemblies for 2014–2021 Toyota Tundra Double Cab and CrewMax vehicles may have been improperly rolled during manufacturing. This can cause the air bag to deploy incorrectly in a crash, increasing the risk of injury.

Moderate·NHTSA·Jul 29, 2026

Certain side curtain air bag assemblies sold as replacement parts for 2016–2023 Toyota Tacoma vehicles may not be properly secured to their mounting bracket. This can cause the air bag to deploy incorrectly during a crash, increasing the risk of injury.

Moderate·NHTSA·Jul 29, 2026

Lidl US is recalling Eridanous Shortbread Cookies with Chocolate Truffle Coating & Apricot Filling (11.6 oz box, UPC 4056489125839) because the packaging has foreign language text only and does not clearly list wheat, soy, milk, and egg allergens in English. People with allergies or sensitivities to these ingredients could have serious reactions.

Moderate·FDA·Jul 24, 2026

Tosoh Bioscience recalled certain lots of its ST AIA-Pack Testosterone test due to a quality control issue that can produce falsely high or falsely low testosterone measurements. Inaccurate results may lead to unnecessary follow-up testing or delayed diagnosis.

Moderate·FDA·Jul 22, 2026·Tosoh Bioscience

The Photera 400 ultraviolet phototherapy device uses a sensor to measure and control UV output for treating skin disorders. A calibration error caused the sensor to report incorrect UV levels, which means patients may have received different doses than intended.

Moderate·FDA·Jul 22, 2026·Daavlin3 products

Maquet (now Getinge) identified that 205 units of the Vasoview Hemopro 2 endoscopic vessel harvesting system from a single lot were exposed to an incorrect sterilization dose during gamma sterilization processing. This occurred at a STERIS facility in New Jersey in late March 2026. The affected devices may not be adequately sterilized.

Moderate·FDA·Jul 22, 2026

3B Medical is recalling Rio II nasal pillows interfaces due to a packaging and labeling discrepancy affecting product size identification and device identifiers. The affected units have incorrect or mismatched labeling on certain lots, which could lead to patients receiving the wrong size for their CPAP or PAP therapy device.

Moderate·FDA·Jul 22, 2026·3B Medical

Medtronic is recalling two cardiopulmonary bypass cannula products after receiving two complaints of loose foreign material, which was confirmed to contain trace amounts of blood. No injuries have been reported. The recall covers two products and was distributed nationwide in several US states as well as worldwide.

Moderate·FDA·Jul 22, 20262 products

Medline is recalling two total knee kits, with 163 units of each, because the Zimmer Biomet mixing bowls and spatulas packed inside were recalled for seal problems that could break sterility. Distribution was limited to California and Utah. No injuries have been reported, and the likely health effect is a short delay in surgery while another device is found.

Moderate·FDA·Jul 22, 20262 products

Papablic is recalling two models of replacement brush heads because the brush heads may break. No injuries have been reported. About 28,100 packs are included in the recall across both models, which were distributed nationwide.

Moderate·FDA·Jul 22, 2026·Papablic2 products

Orthofix is recalling four MiniRail external fixation devices, 161 units in total, because some units may carry the wrong model number. The M101 and M103 labels may be swapped, and some M122 units may be labeled M111. No injuries have been reported.

Moderate·FDA·Jul 22, 20264 products

GE HealthCare found that some Optima XR200, XR220, and XR240amx mobile X-ray systems that had a column replacement may not have had their safety pawl tested to confirm proper assembly. If the internal counterpoise cable fails, the column safety mechanism may not work, and the X-ray tube and collimator arm could drop down the column during an exam. The recall covers 66 units across three products. No injuries have been reported.

Moderate·FDA·Jul 22, 20263 products

Boston Scientific's Rapid Refill Continuous Injection System contains a recalled syringe component that may loosen or disconnect from the device manifold. This could result in fluid leakage, inability to inject or aspirate properly, or complete separation of the syringe, potentially requiring device replacement and extending the procedure.

Moderate·FDA·Jul 22, 2026

Arm drapes used with Intuitive Surgical's da Vinci SP robotic surgical system may detach from the instrument arm due to a defect in the drape rings at the top of the product. If a drape detaches during surgery, it can expose part of the instrument arm and may delay the procedure or require switching to an alternative surgical approach.

Moderate·FDA·Jul 22, 2026

Olympus is recalling four evacuator products, including Toomey and Ellik models, because some sterilization instructions may not reliably make the devices fully sterile. The recall covers about 8,250 units distributed in the US and internationally.

Moderate·FDA·Jul 22, 20264 products

Glass fragments were found in Gellert Global Group Ruby brand artichoke hearts (5 lb 8 oz cans). The affected product was distributed to New York, Pennsylvania, New Jersey, and Connecticut. About 1,150 cases are involved.

Moderate·FDA·Jul 22, 2026·Ruby

OLA-OLA Pounded Groundnuts (Intwilo) 32 oz. packages contain peanuts that are not listed on the label. People with peanut allergies could have a serious reaction if they consume this product. The affected lots (L536531 and L500505) with expiration date 12/28 were distributed in Texas.

Moderate·FDA·Jul 22, 2026

Amy's Kitchen organic lentil soup (light in sodium, 14.5 oz cans) with lot code 60D0924 and best-before date of April 2027 may spoil before the printed date. The affected product was distributed across the U.S. and Canada.

Moderate·FDA·Jul 22, 2026·Amy's Kitchen

W.Y. Industries is recalling duck sauce packets after discovering they may contain metal fragments. The affected packets are 0.35 oz. flexible film packets sold in cases of 500. The issue affects specific lot codes and was distributed to New York, New Jersey, Ohio, and Pennsylvania.

Moderate·FDA·Jul 22, 2026·WY

Winfield's CWB Chocolate Bars in cat, teddy bear, and Easter bunny shapes contain milk that is not listed on the label. People with milk allergies who eat these bars could have a serious allergic reaction. The product was distributed in Houston, Texas.

Moderate·FDA·Jul 22, 2026