New Jersey recalls

Sold nationwide. The radiopaque (X-ray visible) material on the Xact mole marker can detach during use. When this happens, the loose material may create artifacts (unwanted marks or shadows) on mammography images, potentially affecting image quality and interpretation.

Moderate·FDA·Oct 22, 2026·Solstice

Sold nationwide. Medtronic is recalling two product groups in its InterStim system: InterStim SureScan MRI leads and InterStim percutaneous extensions. The recall covers 2 products in total. The company says the wrong lead or extension may have been selected, and an incompatible one may stop the system from working as intended. This could delay surgery or require surgical replacement of the product. No injuries have been reported.

Moderate·FDA·Oct 22, 2026·Medtronic2 products

Sold nationwide. A software bug in MiniMed Go version 1.2.1 broke the long-acting insulin dose reminder feature for users who had it enabled in earlier versions. When users updated the app, the reminder stopped working silently—without any alert to the user. This could cause users to miss or delay insulin doses, or accidentally take a double dose if they're unsure whether they already dosed.

Moderate·FDA·Oct 22, 2026·Medtronic

Sold nationwide. Sixteen restor3d MTP foot implants were distributed without proper sterilization. The implants showed orange sterilization indicators, meaning they were never exposed to the sterilization process required to make them safe for surgery. These implants are used to treat arthritis and other conditions in the big toe joint.

Moderate·FDA·Oct 22, 2026·Restor3d

Sold nationwide. Boston Scientific is recalling 41 Direxion Torqueable Microcatheter models. The hydrophilic coating on the outer tip may not have been fully cured, and some nitinol sleeves have raised ridges caused by laser-cutting misalignment. No injuries have been reported.

Moderate·FDA·Oct 22, 2026·Boston Scientific41 products

Sold nationwide. The Ion Torrent Genexus Dx DNA/RNA sequencing system software (version 6.8.2.1 and earlier) contains security vulnerabilities that could potentially be exploited. Life Technologies has identified 16 affected sequencers across multiple U.S. states.

Moderate·FDA·Oct 22, 2026·Life Technologies

Sold nationwide. Stability testing found that ammonia (NH4+) measurements in specific lots of this quality control material drift over time, making the labeled shelf-life claim unreliable. Labs using affected lots may get delayed or inaccurate results, which could delay diagnosis of dangerously high ammonia levels that need urgent treatment.

Moderate·FDA·Oct 22, 2026·Techno-Path Manufacturing3 products

Sold nationwide. Certain batches of CooperVision Softmed Breathables Advanced Toric contact lenses have incorrect packaging labels stating they are approved for extended wear. These lenses are designed and FDA-approved for daily wear only, not extended wear. The mislabeling could lead users to wear the lenses longer than intended.

Moderate·FDA·Oct 22, 2026·CooperVision

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