Hawaii recalls

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

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

Nutricia is recalling two meal replacement peptide formulas in 12 oz pouches, Liquid Hope and Nourish, both in Berry Medley flavor and sold under the functional formularies name. The company found that the testing lab used the wrong method, which overstated the vitamin A content, so the products may contain less vitamin A than the label states. No injuries have been reported.

Moderate·FDA·Jul 22, 2026·Liquid Hope2 products

Sold nationwide. BD ChloraPrep Clear, a sterile skin antiseptic solution used before medical procedures, may have open or incomplete seals on individual applicator packaging. This could allow contamination of the sterile product. The issue affects multiple lot numbers distributed nationwide.

Moderate·FDA·Jul 22, 2026·CareFusion

Sold nationwide. Chiesi USA is recalling specific lots of CLEVIPREX (clevidipine) injectable emulsion because the manufacturer cannot guarantee the vials are sterile. This affects vials distributed nationwide with lot numbers 1239521 and 1237454, expiring in October 2027. No injuries have been reported.

Moderate·FDA·Jul 22, 2026·Chiesi

Sold nationwide. Bell Pharmaceuticals is recalling 11 carbamide peroxide 6.5% ear drop products, all 0.5 fl oz (15 mL), sold under store and pharmacy brands. Testing found the drops contain far less active ingredient than the label states, and their acidity is also off. No injuries have been reported.

Moderate·FDA·Jul 22, 2026·Bell Pharmaceuticals11 products

Sold nationwide. Padagis Nystatin Cream USP (100,000 units, 15 g tube, lot #205060, expiring 09/30/2027) has been recalled because stability testing found the active ingredient fell below the required strength specification. The cream may not work as effectively as intended to treat fungal infections.

Moderate·FDA·Jul 22, 2026·Padagis

Sold nationwide. PT Organics Limited is recalling select 4 oz. Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit puree pouches sold at Kroger, Meijer, and Target between March and July 2026. An internal packaging defect may have allowed a strand of soft, food-grade plastic to enter some pouches. No injuries have been reported.

Moderate·FDA·Jul 21, 2026·PT Organics

Sold nationwide. Zen Principle Moringa Capsules dietary supplement may be contaminated with Salmonella due to contamination in the moringa leaf powder ingredient. The affected product is Lot A6FF4 with a Best By date of 11/2028, distributed nationwide from December 2025 through July 2026 primarily online. No illnesses have been reported.

Serious·FDA·Jul 19, 2026·Relay Peak Research LLC

Sold nationwide. Four lots of Unique Pharmaceutical Cetirizine Hydrochloride 5 mg tablets were found to be cross-contaminated with ranitidine. The contamination was discovered when pharmacy staff noticed red discoloration on some tablets. People with sensitivity to ranitidine could experience serious allergic reactions.

Serious·FDA·Jul 18, 2026·Unique Pharmaceutical Laboratories

Sold nationwide. MNIENT brand adult portable bed rails (model LQX-110055) do not meet safety standards and can trap users between the rail and mattress, posing a serious risk of injury or death by asphyxiation. The rails also have stability problems and incorrectly sized pins that can cause cuts.

Serious·CPSC·Jul 16, 2026·MNIENT

Sold nationwide. Decorative pearls on Target's Cat & Jack children's sandals can fall off and pose a choking risk to young children. The tan sandals with raffia straps and gold buckles were sold in sizes 5T through 12T from January through May 2026. Target has received 23 reports of pearls falling off, though no injuries have been reported yet.

Serious·CPSC·Jul 16, 2026·Target

Sold nationwide. SDADI wooden kitchen step stools can collapse or tip over during use. Children's bodies can also fit through openings on the front and back, creating a risk of entrapment. The company has received reports of eight tip-overs, including four injuries.

Serious·CPSC·Jul 16, 2026·SDADI

Sold nationwide. Noerishia adult portable bed rails (Model KDB-504B) can trap users between the rail and mattress, or within the rail itself, creating a serious risk of asphyxiation and death. The rails also lack required hazard warning labels and do not meet federal safety standards.

Serious·CPSC·Jul 16, 2026·Hurzein

Sold nationwide. Jobon butane torch lighters do not have the child-resistant safety mechanism required by U.S. law, creating a risk of serious injury or death from fire and burns. The lighters have a side ignition trigger and hands-free operation lock, and come in gray/brown, gold/black, and camouflage print. Approximately 13,200 units were sold online from April 2021 through September 2025.

Serious·CPSC·Jul 16, 2026·Jobon Official Store

Sold nationwide. Madewell Double V-Neck Pullover and V-Neck Cardigan sweaters violate federal flammability standards for clothing textiles, posing a risk of burn injury. One sweater has been reported to catch fire, though no injuries have occurred so far.

Serious·CPSC·Jul 16, 2026·J.Crew