Check a product

Certain 2013–2027 New Flyer buses have an instrument panel indicator light that may not illuminate when the hazard warning lights are on. Without this visual reminder, drivers might forget to turn off the exterior lights, leaving hazard lights active and potentially confusing other drivers.

Moderate·NHTSA·Oct 5, 2026·New Flyer of America, Inc.

Certain 2021 Greenpower Nano Beast school buses have a software error that may allow the bus to move while the wheelchair lift is deployed. This poses a risk of injury to passengers using the lift.

Moderate·NHTSA·Oct 5, 2026·Greenpower Motor Company Inc.

Stewart's Shops Corp. recalled two flavors of half-gallon ice cream—Heavenly Medley and Vanilla-Chocolate-Strawberry—sold in New York, Vermont, and New Hampshire between July and October 2026 because they may contain metal. A consumer found a metal object in one carton. No injuries have been reported.

Moderate·FDA·Oct 2, 2026·Stewart's Shop

Flowers Foods recalled Nature's Own Hawaiian Bread (20 oz. and 40 oz. bags) because the packaging does not list milk as an ingredient, even though milk is present in the product. People with a milk allergy or sensitivity could have a serious allergic reaction if they eat this bread. No illnesses have been reported so far.

Moderate·FDA·Oct 2, 2026

Certain 2022–2024 Blue Bird All American Electric transit buses have high voltage battery mounting bolts that may be loose or missing. This can cause a loss of drive power and increase the risk of a crash.

Moderate·NHTSA·Oct 2, 2026

Certain 2020–2022 Ring Power Terex General 65, C6000, C4000, and TC55 vehicles may have been installed with a pintle hitch that lacks proper reinforcing bracing. If the hitch fails, it can cause the trailer to become uncontrolled, increasing the risk of a crash.

Moderate·NHTSA·Oct 2, 2026·Ring Power Corporation

Altec aerial devices and digger derricks sold between 2020 and 2026 may have a platform access step with improper welds. The step could separate or become unstable during use, creating a fall or injury risk.

Moderate·NHTSA·Oct 2, 2026

Certain 2027 Mercedes-Benz CLA 220 vehicles have a left front seat belt with an incorrectly installed component. This defect may prevent the seat belt from properly restraining occupants in a crash.

Moderate·NHTSA·Oct 2, 2026·Mercedes-Benz USA, LLC

Saint Francis Apizza LLC recalled frozen pizzas in four varieties (Pepperoni, Plain Cheese, Supreme, and Mushroom and Onion) because soy allergen was not listed on the label. The soy comes from soybean oil and soy lecithin in the product. No illnesses have been reported.

Moderate·FDA·Oct 1, 2026

Dollar Tree's electric balloon pump (model 406198) can overheat during use, creating a burn risk. The firm has received three reports of overheating, including one involving flames and one explosion, though no injuries have been reported so far.

Moderate·CPSC·Oct 1, 2026

The front bolt in the seat post clamping mechanism on certain Urban Arrow cargo electric bikes can break, causing the seat to loosen during use. This poses a fall hazard to riders. The manufacturer has received nine reports of damage to the seat-post connection, though no injuries have been reported yet.

Moderate·CPSC·Oct 1, 2026

Certain 2025–2027 Freightliner Business Class M2 trucks have underbody insulation that may contact hot exhaust components, creating a fire risk. Daimler Trucks North America is working on a fix. No injuries have been reported.

Moderate·NHTSA·Oct 1, 2026

Certain 2026–2027 Airstream Rangeline RVs may have a fairing (exterior panel) that can detach due to inadequate adhesion. A detached fairing can fall onto the road and create a hazard for other vehicles.

Moderate·NHTSA·Oct 1, 2026·Airstream, Inc.

Certain 2023–2025 Honda VT1300CX and 2024–2025 VT750 motorcycles have a fuel pump that may malfunction due to a manufacturing defect. If the fuel pump fails, the engine can stall while riding, which increases the risk of a crash.

Moderate·NHTSA·Oct 1, 2026

Certain 2027 Thomas Built SAF-T-LINER C2 and C2 Jouley school buses have a software error that may cause the low beam headlights to not illuminate properly. Insufficient headlight brightness can reduce driver visibility and increase crash risk.

Moderate·NHTSA·Oct 1, 2026

The intake and grille bezels on certain 2026–2027 Mack Anthem AN and 2025–2027 Pioneer PR vehicles may come loose and detach. A loose bezel can fall onto the road and create a hazard for other drivers.

Moderate·NHTSA·Oct 1, 2026

The hitch tube weld on certain Kuat Pivot V3 swing-away hitch adapters can crack, causing the cross beam to detach. A detached cross beam can become a road hazard and increase the risk of crashes for other vehicles.

Moderate·NHTSA·Oct 1, 2026·KUAT INNOVATIONS LLC

Medline is recalling three convenience kits, 1,057 kits in total, because their neurological sponges may contain endotoxin levels that vary unpredictably. Elevated endotoxin can cause reactions such as fever, local inflammation, low blood pressure, or nausea, and may need medical care. No injuries have been reported.

Moderate·FDA·Sep 30, 20263 products

Baxter is recalling three PRO+ MRS mattress surface products, 999 units in total, because the product description on the Unique Device Identification (UDI) label contains errors. The mismatched labels could lead to incorrect product identification or selection, potentially resulting in use with an incompatible bed frame. No injuries have been reported.

Moderate·FDA·Sep 30, 20263 products

Halyard IV START KIT NON-STERILE kits containing BD ChloraPrep Clear applicators may have open or incomplete seals on the applicator packaging. This affects 192 kits (4 cases) with lot number 1642214 and expiration date 7/31/2027. No injuries have been reported.

Moderate·FDA·Sep 30, 2026

New York Embroidery Studio's Trinity Non-Surgical Isolation Gown (Model NYES100-2, X-Large) does not consistently provide the liquid-barrier protection it should. This means the gown may allow fluids to pass through when it should block them, potentially exposing the wearer.

Moderate·FDA·Sep 30, 2026·New York Embroidery Studio

Intervascular's Cardioroot Woven Collagen Coated Vascular Graft failed to meet water permeability specifications in certain batches. The graft is a surgical implant used in vascular procedures. Approximately 16,329 units distributed worldwide are affected.

Moderate·FDA·Sep 30, 2026·Intervascular

During manufacturing quality testing, contamination in Baxter's test equipment may have affected the accuracy of nebulizer flow rate measurements on two VOLARA Homecare devices. The company has retrieved the affected units and retested them; both met specifications.

Moderate·FDA·Sep 30, 2026

DeRoyal Industries myocardial temperature probes (400 Series, Lot #63426754) contain an 18mm needle instead of the correct 15mm needle. This mismatch could affect proper placement and function during cardiac temperature monitoring.

Moderate·FDA·Sep 30, 2026·DeRoyal

Cardinal Health is recalling 2 groups of Presource Convenience Kits, totaling about 26,983 kits, because the applicators inside may have an open or incomplete seal on their packaging. A possibly contaminated applicator could cause no harm, or could lead to a localized skin or soft tissue infection, and less commonly a more widespread infection. The kits were distributed nationwide, with the recall covering stock sent to FL, KY, MO, NC, OH, and TX, and no injuries have been reported.

Moderate·FDA·Sep 30, 20262 products

Some Criticare nGenuity Patient Monitors with CO2 monitoring display a "Checkline Error" alarm during setup, which disables the CO2 monitoring function. This may delay medical procedures that rely on this monitoring capability.

Moderate·FDA·Sep 30, 2026·Criticare

Abiomed has issued a retrospective recall of certain Automated Impella Controller (AIC) units manufactured before 2019. The devices contain firmware and software defects that can affect the accuracy of pressure signals, cause unreliable placement detection, and trigger false alarms. These issues were remedied through firmware and software patches released in 2019.

Moderate·FDA·Sep 30, 2026

Becton Dickinson has recalled certain ForeSight Elite tissue oximetry cables due to incorrect labeling of Channel 1 and Channel 2 on the module and flag labels. This labeling error could cause clinicians to misread oxygen saturation data if the cables are connected to the wrong channels. The affected cables were distributed to hospitals and healthcare facilities.

Moderate·FDA·Sep 30, 2026

A software issue in Philips EPIQ Elite ultrasound systems (Model 795234, software version 14.0) causes doppler blood flow measurements to display at incorrect depths. This can lead to inaccurate velocity readings and potential misdiagnosis of vascular conditions. About 219 units are affected worldwide.

Moderate·FDA·Sep 30, 2026

A small number of Pearle Vision 1 day contact lenses in one affected lot were manufactured with incorrect lens power. This could result in blurred or distorted vision if the wrong lens is worn. No injuries have been reported.

Moderate·FDA·Sep 30, 2026·CooperVision