Colorado recalls

Sold nationwide. 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

Sold nationwide. 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·Ascend Laboratories

Sold nationwide. 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

Sold nationwide. 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

Sold nationwide. 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, 2026·529 Commerce

Sold nationwide. Sunny Pharmtech is recalling three lots of Cyclophosphamide for Injection (1g and 2g vials) distributed between May 2024 and October 2024 because steel particles were found in the product. No injuries have been reported so far, but steel particles in an intravenous injection could cause serious complications including blood clots and infection.

Serious·FDA·Jul 24, 2026·Sunny Pharmtech

Sold nationwide. Baxter is recalling one lot of Cefazolin in Dextrose Injection (a frozen antibiotic infusion bag) because cardboard particles were found in the solution. The affected lot (LD175708, expiring February 14, 2027) was distributed between March and June 2025. No injuries have been reported so far.

Serious·FDA·Jul 24, 2026·Baxter

Sold nationwide. American Regent identified glass and paraformaldehyde particles in one lot of Papaverine Hydrochloride Injection (Lot #25202), a prescription medication used to improve blood circulation and treat muscle spasms. The particles could cause local irritation, blood vessel blockage, and serious complications including stroke.

Serious·FDA·Jul 24, 2026·American Regent

Sold nationwide. Snaps on Peony Design personalized baby bibs and stroller bags can detach, creating a choking hazard for young children. The bibs feature scalloped edges and personalized embroidery, while stroller bags have two snap-closure straps. About 52 items were sold online through Etsy between October 2025 and July 2026.

Serious·CPSC·Jul 23, 2026·Peony Design

Sold nationwide. CuddleCubs Creations teething toy sets sold on Amazon contain pull-string toys with silicone strings that are longer and smaller than safety standards allow. These strings can reach the back of a child's throat and become lodged, creating a serious choking hazard.

Serious·CPSC·Jul 23, 2026·YouRfocus

Sold nationwide. OeyUoc white pool drain covers sold on Amazon do not meet federal safety standards for drain protection and pose a serious risk of entrapment and drowning. The covers violate the Virginia Graeme Baker Pool and Spa Safety Act, which requires drain covers to prevent people—especially children—from getting trapped.

Serious·CPSC·Jul 23, 2026·Yuanxinxiang

Sold nationwide. Sviyatp white pool drain covers do not meet federal safety standards and pose a risk of entrapment and drowning. The covers were sold online as replacement drain covers for swimming pools from March through June 2026.

Serious·CPSC·Jul 23, 2026·Sviyatp

Sold nationwide. Aojieni Silicone pull string teething toys have silicone strings that are longer and smaller than safety standards allow. The strings can reach the back of a child's throat and become lodged, creating a serious choking hazard. One child experienced gagging when the strings reached their throat.

Serious·CPSC·Jul 23, 2026·Segmart

Sold nationwide. Romorgniz 12-drawer fabric dressers sold on Amazon are unstable and can tip over if not anchored to a wall, creating a serious injury or death risk to children. The dressers do not meet federal safety standards for clothing storage units.

Serious·CPSC·Jul 23, 2026·Xuzhou Mingquanhe

Sold nationwide. EnHomee 9-Drawer Fabric Dressers can tip over and trap children if not anchored to the wall. The dressers do not meet federal safety standards required for clothing storage units. About 16,800 units were sold online through Walmart.com between September 2023 and March 2026.

Serious·CPSC·Jul 23, 2026·Xuzhou Mingquanhe

Sold nationwide. 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

Sold nationwide. 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

Sold nationwide. 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·Maquet

Sold nationwide. 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

Sold nationwide. 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, 2026·Medtronic2 products

Sold nationwide. 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, 2026·Medline2 products

Sold nationwide. 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, 2026·Orthofix4 products

Sold nationwide. 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, 2026·GE3 products

Sold nationwide. 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·Boston Scientific

Sold nationwide. ICU Medical is recalling two infusion pump products, the Plum Duo and Plum Solo Precision IV Pump, because in a specific scenario the pump may not count down the Volume to be Infused on its Delivery screen and could deliver up to twice the programmed volume at the set rate. The recall covers about 17,584 units distributed across the US and Canada, and no injuries have been reported.

Serious·FDA·Jul 22, 2026·ICU Medical2 products

Sold nationwide. 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·Intuitive Surgical

Sold nationwide. 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, 2026·Olympus4 products

Sold nationwide. Argon Medical Devices is recalling six procedure trays and kits, including the Transvenous Pacing Electrode Tray, One-Piece Introducer Tray, General Biopsy Tray, T-Lok Bone Marrow Tray, Arterial Line Kit, and Bone Marrow Tray. Some kits contain lidocaine ampules that are already subject to another recall, and the kits did not meet sterility release criteria. No injuries have been reported.

Serious·FDA·Jul 22, 2026·Argon Medical Devices6 products

Sold nationwide. Abiomed is recalling 13 Impella heart pump sets and introducer kits because the introducer sheath may leak from under the sheath cap and along the hub score lines. The problem affects 14Fr and 23Fr introducers, which come in every pump set, and users cannot see it visually. No injuries have been reported.

Serious·FDA·Jul 22, 2026·Abiomed13 products