Alaska recalls

Sold nationwide. These LED finger light toys contain button cell batteries that children can easily access and swallow. Swallowing button cell batteries can cause serious internal injuries, including chemical burns, and can be fatal.

Serious·CPSC·Jul 2, 2026·POPOOO

Sold nationwide. CVS Health Medicated Hemorrhoidal Wipes contain lidocaine and are required to have child-resistant packaging by federal law, but this product does not. Young children could open the wipes and ingest the contents, causing serious injury or death. No injuries have been reported.

Serious·CPSC·Jul 2, 2026·Diamond Wipes

Sold nationwide. Topyond pool drain ports with covers do not meet federal safety standards and pose a risk of entrapment and drowning. The plastic drain ports (model SP-2850V) were sold online starting in May 2024 and do not provide adequate protection against the hazards they are designed to prevent.

Serious·CPSC·Jul 2, 2026·Topyond

Sold nationwide. Vevor baby loungers have sides that are too low to safely contain an infant and openings at the foot that are wider than safety standards allow. The loungers also lack a stand, creating a fall hazard if placed on elevated surfaces. These defects violate mandatory infant sleep product safety standards and can cause serious injury or death.

Serious·CPSC·Jul 2, 2026·Vevor

Sold nationwide. Kao USA recalled select lots of Oribe Serene Scalp Densifying Shampoo (8.5 oz and 33.8 oz) made between February 21–26, 2026 after detecting Pluralibacter gergoviae bacteria. People with weakened immune systems may be at higher risk of infection.

Moderate·FDA·Jul 1, 2026·Kao

Sold nationwide. Eunha Fisheries is recalling certain sliced Korean halibut and flounder sashimi products because the included soy sauce and vinegar red pepper paste packets contain wheat, soy, and sesame allergens that are not labeled on the individual condiment packets themselves. People with allergies or sensitivities to these allergens could have a serious or life-threatening reaction.

Moderate·FDA·Jul 1, 2026·Eunha Fisheries

Sold nationwide. Abiomed is recalling four Impella CP product sets that include 14 Fr Low Profile Introducer Kits, with 195 affected units in total. The introducer may form blood clots (thrombus) during prolonged use. No injuries have been reported, and the distribution covers the US states of FL, IL, MN, NJ, NY, and VA, plus Japan.

Serious·FDA·Jul 1, 2026·Abiomed4 products

Sold nationwide. Medline is recalling 16 convenience kits that contain 10mL polycarbonate colored syringes. The company found design changes to these kits that were not cleared by the FDA, and the products were not included in an earlier report. The kits were shipped nationwide and to Barbados, and no injuries have been reported.

Moderate·FDA·Jul 1, 2026·Medline16 products

Sold nationwide. Boston Scientific has recalled one INTERA 3000 Hepatic Artery Infusion Pump (model AP-0300H) due to the potential for leakage along the drug pathway from the pump through the catheter end. This is an implantable device used to deliver medication directly to the liver. The affected device was distributed in Ohio.

Moderate·FDA·Jul 1, 2026·Boston Scientific

Sold nationwide. Philips Telemetry Monitor 5500 (model 867232) devices may unexpectedly reset to a default state, causing them to lose their configuration settings and disconnect from the hospital's central monitoring system. This could prevent the monitor from reconnecting to the PIC iX central system until manually reconfigured.

Moderate·FDA·Jul 1, 2026·Philips

Sold nationwide. Zimmer discovered that 12 units of the Persona Revision Trabecular Metal Femoral Distal Augment (Model 42-5572-066-10, Size 9/9+, 10mm thickness) contained an incorrect posterior augment component in the package instead of the correct distal augment. No patient injuries have been reported.

Moderate·FDA·Jul 1, 2026·Zimmer Biomet

Sold nationwide. Medtronic recalled three models of its Octopus tissue stabilizers, covering 1,012 units in total. During manufacturing, the company found that the tubing was attached backwards, with the short tube on the bottom of the canister and the long tube on top. No injuries have been reported.

Moderate·FDA·Jul 1, 2026·Medtronic3 products

Sold nationwide. Certain lots of Dexcom G7 continuous glucose monitoring sensors that were designated for destruction were stolen and later sold to pharmacies and distributors without authorization. Two affected lots have different risks: one was not properly sterilized and poses an infection risk, and the other may not provide accurate readings or detect dangerous blood sugar levels.

Moderate·FDA·Jul 1, 2026·Dexcom

Sold nationwide. Surgify Medical is recalling 19 Surgify Halo drill burr products used in bi-portal endoscopic spinal surgery because the burrs may break during use. The recall was filed as a Class II device recall, and no injuries have been reported. The products were distributed nationwide, including to MN, MA, IN, LA, CA, NY, and FL.

Moderate·FDA·Jul 1, 2026·Surgify Medical19 products

Sold nationwide. A software issue in the Thuvera Laser Console (Software Version 2.2) causes the device to display a false error code 5018. This anomaly may lead clinicians to misinterpret the device status during operation.

Moderate·FDA·Jul 1, 2026·IPG Medical

Sold nationwide. GE Healthcare's AW Server 3.2 ext.6.5 has a software issue that can cause the system to display a previous patient's medical images instead of the correct patient's images when launching certain applications. There is no warning or error message when this happens. If a radiologist or clinician does not notice the error, they could misread images, make wrong diagnoses, or recommend incorrect treatment.

Moderate·FDA·Jul 1, 2026·GE

Sold nationwide. Stryker Neurovascular's INZONE Detachment System devices may experience premature battery drain, causing them to fail to power on, display faint indicators, or be unable to detach an embolization coil as intended. If a device fails during a procedure, medical staff may need to use an alternative technique to complete the intervention.

Moderate·FDA·Jul 1, 2026·Stryker

Sold nationwide. Acumed Hexalob Screws used in wrist fixation systems may break during use due to a manufacturing error. The affected screws come in various sizes (2.7mm and 3.0mm) and have been distributed nationwide. No injuries have been reported.

Moderate·FDA·Jul 1, 2026·Acumed

Sold nationwide. Zimmer Biomet is recalling five Off-Axis shoulder system reamer guide products distributed nationwide. The company received five complaints that the plastic guides caught during reaming and broke. No injuries have been reported.

Moderate·FDA·Jul 1, 2026·Zimmer Biomet5 products

Sold nationwide. PFM Medical's Multi-Snare Set catheters (5 mm and 10 mm models) failed to meet biocompatibility safety standards. If used, the device material could cause localized inflammation and tissue irritation when in contact with blood vessels.

Moderate·FDA·Jul 1, 2026·PFM Medical

Sold nationwide. Ventec Life Systems' VOCSN+Pro respiratory ventilator may have a damaged backup battery that powers the alarm system. If primary power is lost and the backup battery is depleted or absent, the backup alarm may not sound to alert caregivers of the power loss.

Serious·FDA·Jul 1, 2026·Ventec Life Systems

Sold nationwide. TMJ Solutions Inc. has recalled one custom temporomandibular joint implant (model CHG020) that may contain incorrect patient-specific components. The mismatch caused a poor fit, resulting in a right-sided open bite for the affected patient.

Moderate·FDA·Jul 1, 2026·TMJ Solutions

Sold nationwide. Philips is recalling two Avalon fetal monitor models, the FM20 and FM30, because the speaker connector may have been assembled incorrectly. Device cables can be pulled out of the housing, which may cause intermittent or permanent loss of speaker output. The recall includes 454 affected units, and no injuries have been reported.

Moderate·FDA·Jul 1, 2026·Philips2 products

Sold nationwide. Certain Da Vinci surgical systems were distributed with a defective E-brake retainer pin. If the structural column fails, this pin can prevent the E-brake from engaging, potentially causing uncontrolled motion of the robotic arm. The pin may also loosen or back out, restricting arm movement or causing uncontrolled motion that could injure patient tissue.

Serious·FDA·Jul 1, 2026·Intuitive Surgical

Sold nationwide. Medline is recalling four groups of convenience kits, 7,738 units in total, because they include lidocaine and bupivacaine injections from supplier Arrow. Those injections were recalled after an FDA inspection of the supplier found quality issues. No injuries have been reported.

Serious·FDA·Jul 1, 2026·Medline4 products

Sold nationwide. Pearl Milling Company Original Pancake & Waffle Mix Complete is being recalled because it contains undeclared milk and soy, which are not listed on the label. The product was distributed only in Puerto Rico. No injuries have been reported.

Serious·FDA·Jul 1, 2026·Pearl Milling Company

Sold nationwide. Spring & Mulberry is recalling 11 flavors of its 2.1 oz date-sweetened chocolate bars, including Mint Leaf, Mixed Berry, Earl Grey, Pure Dark, Pecan Date, and Blood Orange, because they may be contaminated with Salmonella. The bars were sold nationwide, and no illnesses have been reported.

Serious·FDA·Jul 1, 2026·Spring & Mulberry11 products

Sold nationwide. Motor City Pizza Co. 5 Cheese Bread products may contain Salmonella, a bacteria that can cause serious illness. The affected products were distributed nationwide to major retailers including Costco, Walmart, Target, and Kroger.

Moderate·FDA·Jul 1, 2026·Motor City Pizza Co

Sold nationwide. Sun Pharmaceutical discovered that some bottles labeled as containing 6mg Perampanel tablets actually contained 10mg tablets instead. This mix-up affects one lot (AE01763) distributed nationwide. Patients taking the wrong strength could receive an incorrect dose of this seizure medication.

Moderate·FDA·Jul 1, 2026·Sun Pharmaceutical

Sold nationwide. Elevate Oral Care's Povi-One 10% Povidone-Iodine Oral Antiseptic does not contain the full strength stated on the label. Five specific production lots distributed nationwide do not meet the required potency standard, which means the product may not work as intended for oral antiseptic purposes.

Moderate·FDA·Jul 1, 2026·Elevate Oral Care