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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, 20263 products

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

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

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

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

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

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

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

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

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, 20262 products

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, 20262 products

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

Evexias Health Solutions Amino Ultra capsules are mislabeled and do not declare fish oil as an ingredient. This poses a risk to people with fish allergies. The recall affects 30 bottles distributed across multiple states.

Moderate·FDA·Oct 21, 2026·Evexias Health Solutions

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

Pur Aqua Sparkling Frost Cherry Limeade 17 oz. bottles may contain aspartame that is not listed on the label. The affected products have a best-if-used-by date of 032327 and were distributed in Florida. Aspartame is an artificial sweetener that must be clearly labeled for consumers who need to avoid it for health reasons.

Moderate·FDA·Oct 21, 2026

Stewart's Shop is recalling two half-gallon ice cream products, Stewarts Shops Vanilla Chocolate Strawberry Ice Cream and Stewarts Shops Vanilla Heavenly Medley, because they may contain pieces of metal. About 21,000 units were sold in New York, Vermont and New Hampshire. No injuries have been reported.

Moderate·FDA·Oct 21, 2026·Stewart's Shop2 products

Daring Foods Plant Steak Bites microwaveable pouches have defective packaging that can rupture or explode during cooking. The affected product has a Best By Date of September 14, 2027 (Lot #2576) and was distributed to grocery stores in Florida and North Carolina.

Moderate·FDA·Oct 21, 2026·Daring Foods

J. HIGGS Loaded Bacon & Cheddar Potato Chips (7.75 oz bags) contain soy that is not listed on the package label. People with soy allergies or intolerances could have a serious reaction if they eat these chips without knowing soy is present.

Moderate·FDA·Oct 21, 2026

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

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

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

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

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

The heater hose in certain 2027 Saf-T-Liner C2 school buses may rupture, causing hot coolant to leak inside the passenger compartment. Contact with hot coolant can burn occupants.

Moderate·NHTSA·Oct 21, 2026

The electronic parking brake on certain 2025–2026 Koenigsegg CC850 vehicles may not engage properly when the vehicle is in reverse. This can allow the vehicle to move unexpectedly, increasing the risk of a crash or injury.

Moderate·NHTSA·Oct 21, 2026·Koenigsegg Automotive AB

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·Cronus Pharma

Two 100% squeezed orange juice products sold in California are being recalled: Voila! juice and Andronico's Community Markets juice, in 16 oz to 128 oz sizes. The juice was not processed to achieve the required 5-log reduction of harmful pathogens. No illnesses have been reported.

Moderate·FDA·Oct 20, 2026·Voila2 products

Trader Joe's Crispy Rice Milk Chocolate Bars (3-pack, imported from Belgium) contain wheat that is not listed on the outer package label. People with wheat allergies or celiac disease who eat these bars without knowing they contain wheat could have a serious allergic reaction. The affected product has lot code LT26189 with a best-by date of 10.08.2027.

Moderate·FDA·Oct 20, 2026

El Ruiseñor De Mexico is recalling 61 products, including Jovy gummy candies and Fritura snacks, plus sesame seeds, almonds, peanuts, dried fruit and shrimp. The products may contain sesame that is not listed on the label, which is a risk for people with sesame allergies. Most were sold in California, with some sent to Hawaii, Illinois, Kansas, Nevada, Oregon and Washington.

Moderate·FDA·Oct 20, 202661 products

Certain 2022–2026 Toyota Sienna Hybrid 7-passenger vehicles have second-row seat backs that may not stay secured during a crash. An unsecured seat back may fail to protect an occupant properly, increasing injury risk.

Moderate·NHTSA·Oct 20, 2026