New Jersey recalls

Sold nationwide. Macleods Pharma USA is recalling specific lots of Olmesartan Medoxomil, Amlodipine, and Hydrochlorothiazide combination tablets (40 mg/10 mg/12.5 mg) because they failed to meet dissolution specifications. This means the tablets may not break down properly in the body, potentially reducing how well the medication works.

Moderate·FDA·Oct 26, 2026·MacLeods Pharma

Sold nationwide. Tonight We Ride, LLC recalled all lots of Ultimate Forza Male Supplement capsules because they contain three undeclared active ingredients: sildenafil and tadalafil (prescription drugs sold as Viagra and Cialis) and dapoxetine (not approved by the FDA). These ingredients were found through third-party testing and pose health risks, especially for people taking nitrate medications or with heart conditions.

Serious·FDA·Oct 24, 2026·Tonight We Ride

Sold nationwide. Certain Ziehm Orthoscan VERSA accessory carts and Versa Mini C-Arm systems have welds that do not meet specifications. This defect could cause the monitor arm mounting structure to separate from the cart during use.

Moderate·FDA·Oct 23, 2026·Ziehm Imaging

Sold nationwide. Medtronic has recalled certain OmniaSecure Model 3930M ventricular leads (used in heart devices for pacing and defibrillation) due to reports of difficulty achieving proper fixation during implantation. This implantation difficulty could potentially cause tissue trauma during the surgical procedure.

Moderate·FDA·Oct 23, 2026·Medtronic

Miyoko's Creamery European Style Salted Plant Milk Butter (8 oz units, UPC 857554005773) has been recalled because some packages may contain yeast, mold, and E. coli. The affected product was distributed to Connecticut, Florida, Georgia, Iowa, Illinois, Indiana, Maryland, New Jersey, New Hampshire, and Wisconsin.

Moderate·FDA·Oct 23, 2026·Miyoko's Creamery

Eden Brothers Broccoli Seeds (Calabrese variety) in 1 oz and 1 pound pouches may be contaminated with Salmonella. The affected product was packed in 2027 under lot numbers 1022067 and 1022068, and was distributed nationwide.

Serious·FDA·Oct 23, 2026·EDEN BROTHERS

Sold nationwide. ZestiGreens Broccoli Seeds for Sprouting & Microgreens (8 oz and 16 oz packages) may be contaminated with Salmonella. The seeds were primarily sold through Amazon. No illnesses have been reported.

Serious·FDA·Oct 23, 2026·ZestiGreens

Sold nationwide. Hikma Pharmaceuticals is recalling Abirtega (abiraterone acetate) 250 mg tablets due to failed weight uniformity specifications. Lot 3047 (expiring July 2027) does not meet quality standards. The issue was identified during quality testing; no injuries have been reported.

Moderate·FDA·Oct 23, 2026·Hikma Pharmaceuticals

Sold nationwide. Safecor Health is recalling specific batches of metoclopramide 5 mg tablets manufactured for Teva Pharmaceuticals due to co-mingled tablets in the bottles. Co-mingling means tablets from different batches or products may have been mixed together. The affected lot is 3116509 with an expiry date of 07/31/2027.

Moderate·FDA·Oct 23, 2026·Safecor Health

Sold nationwide. Glenmark Pharmaceuticals is recalling Abiraterone Acetate Tablets USP 500 mg in 60-count bottles due to a labeling defect. The affected lot (13250135, expiring 11/2027) was distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 23, 2026·Glenmark

Sold nationwide. Ritedose Pharmaceuticals recalled one lot of Formoterol Fumarate Inhalation Solution (20mcg/2mL) because it failed quality testing for impurities and degradation. The affected lot (25BL0, expiring 02/28/2027) was distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 23, 2026·Ritedose

Sold nationwide. Halyard ANTERIOR HIP PACK surgical kits (model SOAH31) contain a component that was not properly sterilized before packaging. The component was placed outside the sterile barrier and did not receive the required sterilization treatment. This affects 56 kits distributed in Arizona with lot number 1689215 and expiration date 11/06/2026.

Moderate·FDA·Oct 22, 2026·AVID Medical2 products

Sold nationwide. Medline is recalling 13 surgical drape and medical convenience kit products because the adhesive can be difficult to remove from patients and may leave residue on the skin. No injuries have been reported. The recall covers US nationwide distribution and several other countries.

Moderate·FDA·Oct 22, 2026·Medline13 products

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