West Virginia recalls

Sold nationwide. EAK Distribution LLC is recalling Heirloom Homegrown Green Sprouting Calabrese Broccoli Sprout Seeds (8 oz packets) sold on Amazon due to potential Salmonella contamination. The affected lot is AUG172026, and approximately 3,600 packets were distributed nationwide.

Serious·FDA·Oct 22, 2026·Heirloom Homegrown

Sold nationwide. Gardeners Basics brand Waltham 29 Broccoli Sprouting Seeds have been recalled due to potential Salmonella contamination. The affected product is packaged in a 1-pound white and green resealable pouch with UPC 848137042889 and marked "Packed for 2027". About 235 bags were distributed nationwide through online sales.

Serious·FDA·Oct 22, 2026·Gardners Basics

Sold nationwide. BAMAMON LED Projecting Finger Light toys contain button cell batteries that can be swallowed, posing a serious injury or death risk to young children. The toys, sold in 32-piece boxes with space-themed projections, violate federal safety standards for toys.

Serious·CPSC·Oct 22, 2026·Bamamon

Sold nationwide. The adjustable tilt arm that holds certain Lithonia Lighting RSX outdoor luminaires to poles or wall brackets can break, causing the fixture to fall. The company has received reports of arm failures and four instances of fixtures falling, though no injuries have been reported so far.

Moderate·CPSC·Oct 22, 2026·Lithonia Lighting

Sold nationwide. Costway convertible high chairs lack a required safety restraint system, allowing children to slip through the gap between the feeding tray and seat. This can lead to entrapment or falls, creating a serious injury or death hazard.

Serious·CPSC·Oct 22, 2026·Costway

Sold nationwide. VQQQ-branded natural gas patio heaters (models VQQQ-A1 and VQQQ-001) can malfunction, causing gas to leak. This poses a risk of serious injury or death from fire and burns. About 100 units were sold online via Amazon between July 2024 and August 2026.

Serious·CPSC·Oct 22, 2026·VQQQ

Sold nationwide. CIYTI Light-Up Princess Costumes contain button cell batteries in the crown, scepter, and remote control that children can access easily. If swallowed, these batteries can cause serious internal injuries or death.

Serious·CPSC·Oct 22, 2026·CIYTI

Sold nationwide. Wedgewood Pharmacy is recalling certain compounded veterinary medications shipped between February and October 2026 because lab testing data was unreliable, meaning some products may be weaker or stronger than intended. The affected medications include powders, pastes, oral liquids, injectables, and topical products for companion, equine, exotic, zoo, and aquatic animals. Wedgewood discovered the issue through its own quality checks and has received 98 complaints, including 7 serious ones.

Moderate·FDA·Oct 21, 2026·Wedgewood Pharmacy

Sold nationwide. Medtronic MiniMed CareLink Clinic software version 4.4A has a defect in its Settings Calculator feature. When healthcare providers enter custom insulin values, the calculator ignores them and continues using default values instead. This can result in incorrect insulin dose recommendations being sent to patients' insulin pumps, potentially causing patients to receive too much or too little insulin.

Serious·FDA·Oct 21, 2026·Medtronic

Sold nationwide. Beckman Coulter has recalled certain SW40 rotors (Reference 331302) used in Optima XE and XPN ultracentrifuges due to a defect that can cause rotors to break during operation. Rotor breakage destroys samples being processed and can expose laboratory workers to biohazardous materials. When used for patient testing, breakage may delay diagnostic results.

Moderate·FDA·Oct 21, 2026·Beckman Coulter2 products

Sold nationwide. Certain Greiner VACUETTE blood collection tubes (lot B26043FM) may be contaminated with EDTA, a chemical that can interfere with test results. This contamination can cause lab tests to show falsely high potassium and falsely low calcium levels, which could lead to serious medical decisions based on incorrect results.

Moderate·FDA·Oct 21, 2026·Greiner Bio-One

Sold nationwide. Radiometer Medical's ABL90 FLEX and ABL90 FLEX PLUS blood analyzers may produce inaccurate test results due to issues with how certain sample types and test parameters are configured. The company has identified that whole blood samples are no longer suitable for two specific tests (FHbF and ctBil), and reportable ranges for some other measurements need adjustment.

Moderate·FDA·Oct 21, 2026·Radiometer Medical

Sold nationwide. Medline Industries recalled a foot-ankle convenience kit (SKU DYNJ65395A) because one component in the kit has an incorrect or discrepant shelf-life label. The issue affects 30 kits distributed in New York. No injuries have been reported.

Moderate·FDA·Oct 21, 2026·Medline

Sold nationwide. Healthmark Industries' vinyl instrument guards have labeling that does not comply with federal requirements under 21 CFR 801. The manufacturer has also updated instructions for steam sterilization of these guards. The recall affects multiple model numbers across various sizes and colors.

Moderate·FDA·Oct 21, 2026·Healthmark Industries

Sold nationwide. IntelePACS, a medical imaging system used in hospitals and clinics, has a software issue where displayed images may not match the printed reports when using certain web browsers. This could lead to confusion during diagnosis or patient care if a clinician relies on mismatched information.

Moderate·FDA·Oct 21, 2026·Intelerad

Sold nationwide. Medline is recalling six convenience kits that contain CONMED AirSeal Access Ports, with 3,551 kits affected for each product listed. The ports may give false overpressure alerts and vent during use, which could delay or end a procedure. The kits were distributed nationwide, including AZ, CA, IN, MD, MO, NJ, OH, and WI, and no injuries have been reported.

Moderate·FDA·Oct 21, 2026·Medline6 products

Sold nationwide. Medline is recalling 12 groups of surgical convenience kits, including cardiac, vascular, spinal, neuro, and ear kits. Some kits contain cannula components that do not meet ISO 80369-7 size requirements, which may cause leaking or breaking during use. No injuries have been reported.

Moderate·FDA·Oct 21, 2026·Medline12 products

Sold nationwide. Howmedica Osteonics is recalling four Triathlon surgical instrument trays, about 2,100 trays in total. The reprocessing instructions call for a 30-minute dry time after sterilizing trays in blue wrap, which may leave a small amount of moisture on the trays. No injuries have been reported.

Moderate·FDA·Oct 21, 2026·Howmedica Osteonics4 products

Sold nationwide. Some LeadCare II Blood Lead Test Kits (model 70-6762, sub-lot 2530M-01) have an incorrect expiration date printed on the outer label. The label shows July 22, 2026, but the correct date is July 13, 2026. When used after the correct expiration date, the system will display an error and prevent the test from running, causing delayed results.

Moderate·FDA·Oct 21, 2026·Magellan Diagnostics

Sold nationwide. Beckman Coulter is recalling DxU 840m and 850m Iris analyzers and several IQ200 Sprint, Select, and Elite analyzer models. The rinse-line check valve on these instruments wears out sooner than expected and needs yearly replacement, but that step was left out of the required preventive maintenance schedule. If the valve is not replaced, lamina fluid can leak onto the table or floor, and no injuries have been reported.

Moderate·FDA·Oct 21, 2026·Beckman Coulter2 products

Sold nationwide. Certain vials of Microgenics MAS Omni IMMUNE PRO Liquid Assayed Integrated Immunoassay Control (Level 1, Lot OPRO29061A) show inconsistent quality from vial to vial. This variability can cause low recovery of parathyroid hormone (PTH) in lab testing, potentially delaying results that are reported to patients and doctors.

Moderate·FDA·Oct 21, 2026·Microgenics

Sold nationwide. Some Gore VIABIL Short Wire Biliary Endoprosthesis devices (models VSWVH0808 and VSWVN1006) may have been labeled with the wrong length. These are small, flexible tubes placed in bile ducts to keep them open. If a doctor uses a device with incorrect length information, it could affect proper placement.

Moderate·FDA·Oct 21, 2026·Gore

Sold nationwide. In2bones USA distributed CoLag bone screws labeled as fully threaded that are actually partially threaded. This mismatch could affect surgical outcomes if the wrong screw type is used during orthopedic procedures. The error affected 29 units distributed across multiple states.

Moderate·FDA·Oct 21, 2026·In2bones

Sold nationwide. The vented cap on this high-level disinfectant bottle can become blocked, causing gas to build up inside. When the pressure increases, the bottle may swell, and opening it could release vapor or liquid that may expose users to the chemical if protective equipment is not properly worn.

Moderate·FDA·Oct 21, 2026·Steris3 products

Sold nationwide. Ethicon surgical sutures were packaged with an alcohol-based fluid that was not part of the product design. If the fluid contacts the suture during surgery, it can weaken the suture's strength and knot security, potentially causing wound complications including bleeding or reopening.

Moderate·FDA·Oct 21, 2026·Ethicon

Sold nationwide. Baxter Healthcare's Likorall overhead patient lifts may experience motor shaft breakage combined with reduced safety system performance, causing the lift strap to lower faster than expected during use. This malfunction could result in patient injury if a significant fall occurs.

Serious·FDA·Oct 21, 2026·Baxter

Sold nationwide. BioFire Diagnostics is recalling specific lots of three infection test panels: the FilmArray Pneumonia Panel, the FilmArray Pneumonia Panel plus, and the BioFire Joint Infection Panel. The lots may be contaminated, which could cause false positive test results. No injuries have been reported, and 9,949 units are listed as affected.

Moderate·FDA·Oct 21, 2026·BioFire Diagnostics3 products

Sold nationwide. Internal testing found that the sterile pad in the FORWARD Gunshot Wound Kit (Model AFT-GSW) may degrade over time. This degradation could cause small pieces of the pad material to come loose and contaminate the wound during treatment.

Moderate·FDA·Oct 21, 2026·Integrated Medcraft

Sold nationwide. SI-BONE discovered that pelvic fixation screws in certain iFuse TORQ Implant System models failed packaging seal integrity testing. This means sterility cannot be guaranteed for the affected units. No injuries have been reported.

Moderate·FDA·Oct 21, 2026·SI-BONE

Sold nationwide. A firmware issue in certain Ferno-Washington Power F2 Powered Fastening Systems can cause the device to intermittently lose or reduce its powered functionality when used with compatible Power X2 stretchers. Affected devices may stop operating in powered mode or perform at reduced power, which could delay or interrupt patient transport.

Moderate·FDA·Oct 21, 2026·Ferno