Idaho recalls

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

Sold nationwide. Sarnova HC assembled some Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipacks (10-pack, Item 670272-KIT, Lot ASM0043314) with pediatric nasal cannulas instead of adult nasal cannulas. This size mismatch could result in incorrect gas sampling or fit during use. About 2,500 kits were distributed across the Midwest and Mountain regions.

Moderate·FDA·Oct 21, 2026·Sarnova

Sold nationwide. Boston Scientific discovered that 403 units of the NaviFlex LW Pusher Advx Panc. Stent were incorrectly manufactured with an extra guidewire exit port that should not be present on this device model. This manufacturing error could affect how the device performs during use.

Moderate·FDA·Oct 21, 2026·Boston Scientific

Sold nationwide. Certain NeuroStar Advanced Therapy System units contain coil assembly cables that do not meet product specifications. The affected coil assemblies are identified by specific serial numbers. This defect could affect the device's performance or reliability during treatment.

Moderate·FDA·Oct 21, 2026·Neuronetics

Sold nationwide. The IOMAX Cortical Module, a medical device used for electrical stimulation testing, contains a defective printed circuit board that may cause the device to deliver electrical stimulation to a patient unintentionally or allow unwanted electrical current to reach the patient. The issue affects 23 devices with specific serial numbers distributed in the US and internationally.

Serious·FDA·Oct 21, 2026·Cadwell

Sold nationwide. Becton Dickinson's Phoenix Panel NMIC-312 (Catalog Number 449082) may produce inaccurate results when testing Klebsiella pneumoniae using the CPO Ambler classification feature. This could cause quality control checks to fail undetected in clinical laboratories.

Moderate·FDA·Oct 21, 2026·Becton Dickinson2 products

Sold nationwide. Medtronic found that the donor tissue used in batch A62881 did not meet its microbial screening requirements, and donor bone tested positive for Clostridium butyricum. Although the tissue was gamma irradiated and the finished batch passed sterility testing, implanting it could lead to a Clostridium infection. The recall covers two products, and no injuries have been reported.

Moderate·FDA·Oct 21, 2026·Medtronic2 products

Sold nationwide. The Jenavalve Trilogy Delivery Catheter (Size 23MM, REF: TRILOGY-DC-S) may experience separation of the sleeve liner, which could make it difficult or impossible to deploy the heart valve device during the procedure. The FDA has classified this as a Class II recall.

Moderate·FDA·Oct 21, 2026·Jenavalve3 products

Sold nationwide. Instrumentation Laboratory is recalling two part numbers of the HemosIL AcuStar HIT-IgG(PF4) in vitro diagnostic test, 1,848 units in total. The test may produce an invalid calibration curve, or patient results may read up to 47% lower than they should. The recall covers US states and countries worldwide. No injuries have been reported.

Serious·FDA·Oct 21, 2026·Instrumentation Laboratory2 products

Sold nationwide. Primal Herbs Volume, sold as a herbal supplement, contains sildenafil—a prescription medication—that is not listed on the label. FDA testing confirmed the presence of this undeclared ingredient. The product was sold online between July 2 and September 19, 2025.

Serious·FDA·Oct 21, 2026·Primal Herbs

Wild West Seed Inc is recalling specific lots of broccoli seeds (Green Sprouting Calabrese lot #4105 and Waltham29 lot #4475) because they may be contaminated with Salmonella. The seeds were distributed across multiple states and the United Kingdom.

Serious·FDA·Oct 21, 2026·Wild West Seeds

Sold nationwide. Walker Foods, Inc. recalled Marca El Pato Salsa para Enchiladas (28 oz cans) because the product contains salt, garlic, and onions that are not listed on the label. People with allergies or sensitivities to these ingredients could be at risk if they rely on the label to make safe choices.

Moderate·FDA·Oct 21, 2026·El Pato

Sold nationwide. Holsum Spinach Flour Tortillas (large, 8-count packages) contain FD&C Blue No. 1 and FD&C Yellow No. 5 food dyes that are not listed on the label. People with sensitivities or allergies to these dyes may be affected. The affected product was distributed in Puerto Rico and the US Virgin Islands.

Moderate·FDA·Oct 21, 2026·Holsum

Sold nationwide. Par Health USA's Dexmedetomidine HCl injection vials contain unwanted particulate matter, identified as cellulose or stopper material. The contamination affects two specific lots distributed nationwide. This is a prescription medication used during anesthesia and sedation.

Serious·FDA·Oct 21, 2026·Paragon 28

Sold nationwide. American Health Packaging distributed metoclopramide 5 mg tablets that contained foreign tablets or capsules mixed in with the correct medication. The contamination was found in two lot numbers distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 21, 2026·American Health Packaging

Sold nationwide. Houston Rx is recalling two injectable products, a tirzepatide/niacinamide 2 mL vial and a sermorelin 10 mL vial, because the company cannot assure they are sterile. The recall covers 71 vials distributed nationwide in the USA, and the FDA has reported no injuries.

Moderate·FDA·Oct 21, 2026·Houston Rx2 products

Sold nationwide. Zydus Pharmaceuticals is recalling specific lots of Hydrocortisone Sodium Succinate for Injection because the drug failed quality testing for impurities and degradation. The affected lots (LB00047A and LB00048A, expiring 03/2028) were distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 21, 2026·Zydus

Sold nationwide. Teva Pharmaceuticals discovered that some bottles of Metoclopramide 5 mg tablets contain foreign tablets or capsules mixed in with the correct medication. The contamination was found in specific lots distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 21, 2026·Teva

Sold nationwide. Ventec Life Systems is recalling 12 ventilator models used for ventilatory support, including VOCSN+Pro, VC+Pro, VOCSN, VCSN+Pro, V+Pro, VC, V+ Pro Emergency and V*Home, some in Japan versions. The internal flow transducer cable connector may disconnect from the internal board, which could cause the system to reboot and interrupt ventilation therapy. The notice reports no injuries, and the devices were distributed nationwide, including Puerto Rico.

Serious·FDA·Oct 20, 2026·Ventec Life Systems12 products

Sold nationwide. Cronus Pharma is recalling one lot of AnaSed Equine Injection (xylazine 100 mg/mL), a sedative for horses, due to reports of product discoloration. The affected lot is C25110AV1 with an expiration date of November 2027. Discoloration may indicate a quality issue with the medication.

Moderate·FDA·Oct 20, 2026·AnaSed

Sold nationwide. WAP Sensual Enhancement Capsules were sold without FDA approval and contain three undeclared prescription medications: sildenafil, tadalafil, and flibanserin. These are potent drugs that require a doctor's prescription and can cause serious health problems, especially in people taking other medications or with certain medical conditions.

Serious·FDA·Oct 20, 2026·Erotic Enhancers

Sold nationwide. Right Value Drug Stores LLC is recalling compounded testosterone cypionate injection (200 mg/mL) in 5 mL and 30 mL vials due to lack of sterility assurance. The affected vials were distributed nationwide to medical offices. No injuries have been reported.

Moderate·FDA·Oct 19, 2026·Right Value Drug Stores LLC

Sold nationwide. Ashtel Studios Inc. of Ontario, California is recalling 17 fluoride toothpaste products nationwide because they were made in ways that did not meet FDA manufacturing standards. The products are sold under the Barbie, Hot Wheels, Crayola and My Little Pony names, plus the Brush Buddies, evo, ARU and BB brands. No injuries have been reported.

Moderate·FDA·Oct 19, 2026·PRITAM INTERNATIONAL PRIVATE LIMITED17 products

Sold nationwide. Kayem Foods discovered that some of its ready-to-eat meat and poultry products may have been stored at unsafe temperatures in a warehouse cooler. The products were made between late March and early October 2026. No illnesses have been reported so far.

Serious·USDA·Oct 17, 2026·Kayem

Sold nationwide. Philips Smart-hopping 2.0 AP wireless access points may experience unreliable roaming behavior when older Smart-hopping 1.0 wireless clients move between locations. This can cause loss of connection to the central monitoring system, potentially interrupting patient monitoring in healthcare facilities.

Moderate·FDA·Oct 16, 2026·Philips

Sold nationwide. Axonics has recalled certain lots of its PNE Lead Implant Kit because the 10mL luer lock syringes included in the kit may leak, break, or malfunction. This could affect the safe use of the implant procedure. The recall affects approximately 18,294 kits distributed nationwide and internationally.

Moderate·FDA·Oct 16, 2026·Axonics

Sold nationwide. Medtronic Navigation is recalling four products: certain NDI passive spheres and a biopsy needle kit. The reflective material on these items may vary, which could affect a navigation system's ability to detect and track them. No injuries have been reported.

Moderate·FDA·Oct 16, 2026·Medtronic4 products

Sold nationwide. B. Braun Medical Inc is recalling certain SAFSITE Injection Site valves (model RV1000NC, catalog number 415068) because they may leak or allow blood to flow backward into the IV line. This could affect the safety of IV therapy. The recall affects specific lot numbers with expiration dates in September and October 2029.

Moderate·FDA·Oct 16, 2026·B. Braun

Sold nationwide. Think Surgical's Square Driver robotic component did not meet design specifications. This could cause the pin to become stuck or wobble during surgical drilling procedures. No injuries have been reported.

Moderate·FDA·Oct 16, 2026·Think Surgical