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BMC Medical Co., Ltd. recalled 20,160 Luna G3 APAP sleep apnea devices (Model LG3600) due to a firmware defect in version G3-2.00.76. Under certain high-pressure, high-breathing-rate conditions, affected devices can display an error message and shut down automatically, stopping therapy delivery. Most devices were corrected with a firmware upgrade, but up to 196 units may still contain the defective version.

Serious·FDA·Sep 7, 2026·BMC Medical

The touchscreen instrument cluster in certain 2024–2027 Can-Am motorcycles may reset, freeze, or go blank, leaving the display unable to show vehicle speed and warning lights. This increases the risk of a crash.

Moderate·NHTSA·Sep 7, 2026·Bombardier Recreational Products, Inc.

Made Fresh Salads Inc. is recalling ready-to-eat deli salads and cream cheese products distributed in New York City because they may be contaminated with Listeria monocytogenes. The contamination was discovered through environmental testing at the facility. No illnesses have been reported so far.

Serious·FDA·Sep 6, 2026

Prime Line Distributors and Ferrarini USA are recalling imported ready-to-eat pork guanciale (cured pork jowl) products that may be contaminated with Listeria monocytogenes. The products were produced in Italy in May 2026 and imported to the U.S. in July 2026. The contamination was discovered during routine testing; no illnesses have been reported.

Serious·USDA·Sep 6, 2026

Certain 2026–2027 Kibbi recreational vehicles equipped with MaxxAir rooftop ventilation fans may have a printed circuit board that can fail and overheat during normal operation. An overheated circuit board creates a fire risk.

Moderate·NHTSA·Sep 5, 2026·Kibbi, LLC

SUPPLX.com's Business Pill and Branch Manager for Men dietary supplements contain yohimbine that is not listed on the labels. FDA testing found dangerously high levels of this substance, which can cause serious heart problems, severe high blood pressure, and other dangerous side effects—especially in people taking stimulants or certain medications.

Serious·FDA·Sep 3, 2026

American Regent is recalling three lots of epinephrine injection (1 mg/mL multi-dose vials) due to leaking and cracked vials, plus contamination with particles including nylon, cellulosic, acrylic, polyethylene, and glass. These particles can block blood vessels, cause blood clots, and damage organs; cracked vials also risk loss of sterility and bacterial contamination. No adverse events have been reported so far.

Serious·FDA·Sep 3, 2026

A coolant sensor in certain 2023–2024 Nova Bus LFS Artic and 2022–2024 LFS buses can send a false signal, causing the engine to shut down without warning. An unexpected shutdown increases crash risk and can create unsafe conditions when passengers need to be transferred from a disabled bus.

Moderate·NHTSA·Sep 3, 2026

A defective coolant level sensor in certain Nova Bus vehicles may send a false signal and cause the engine to shut down unexpectedly while driving. This can increase the risk of a crash and cause injury to passengers during emergency transfer from the disabled bus.

Serious·NHTSA·Sep 3, 2026

Certain Mondraker mountain bicycles equipped with ONOFF S9 Carbon MTB handlebars may have handlebars that crack or fracture during use. This can cause loss of control and a fall. The company has received five reports of handlebar breakage, including two injuries from falls.

Serious·CPSC·Sep 3, 2026

Clorox Puerto Rico is recalling about 6.3 million bottles of scented Mistolin and Lestoil cleaners sold in Puerto Rico and the U.S. Virgin Islands. The products may contain Pseudomonas aeruginosa bacteria, which can cause serious infections in people with weakened immune systems or external medical devices if the bacteria is inhaled, touches the eyes, or enters through a break in the skin. People with healthy immune systems are typically unaffected.

Moderate·CPSC·Sep 3, 2026·Clorox

The lithium-ion battery in XO Poppy Power Trip Magnetic Wireless Power Banks (model PYPBK5M) can overheat and catch fire. About 32,400 units were sold at TJX and Marshalls stores in three colors: cream, cream with pink bow print, and black with teddy bear print. No injuries have been reported.

Serious·CPSC·Sep 3, 2026

The black eyes on this teether can detach when frozen, creating a choking risk for babies. Skip Hop has received four reports of eyes coming off, though no injuries have been reported yet.

Serious·CPSC·Sep 3, 2026

These squishy toys contain water beads that can expand if swallowed, potentially causing choking, intestinal blockage, and serious injury or death. The toys are translucent squishy balls with cartoon faces, sold in tan bamboo steamer-shaped containers.

Serious·CPSC·Sep 3, 2026

OKK Trading's Rainbow Mystery Squishy Bun Toys contain water beads that can expand larger than safe limits. If a child swallows a water bead, it can cause choking, intestinal blockage, and serious injury or death.

Serious·CPSC·Sep 3, 2026

Gizoon Direct six-drawer dressers can tip over if not anchored to the wall, creating a risk of serious injury or death to children. The dressers do not meet federal safety standards for furniture stability.

Serious·CPSC·Sep 3, 2026

The backrests on certain Branch height-adjustable ergonomic chairs can detach due to incorrectly installed anchors at the factory. This poses a fall hazard. The chairs were made between September 10, 2025 and April 22, 2026. Branch has received 11 reports of backrest detachment but no injuries so far.

Moderate·CPSC·Sep 3, 2026

Certain Amana brand through-the-wall air conditioners and heat pumps can develop a short circuit in the snubber component, which may emit flames. Two incidents of this short circuit have been reported, though no injuries have occurred yet.

Serious·CPSC·Sep 3, 2026

Loyoda adult portable bed rails do not meet federal safety standards for adult bed rails. They pose a risk of serious injury or death from entrapment and asphyxiation.

Serious·CPSC·Sep 3, 2026·Loyoda

SHEIN Distribution Corporation is recalling spiral toys that contain small plastic balls. These toys are intended for children under three years old, but the small balls pose a serious choking hazard and violate federal safety rules for that age group.

Serious·CPSC·Sep 3, 2026

The lithium-ion batteries in Cambridge Audio Yoyo (M) Portable Bluetooth Speakers can overheat and catch fire. The company has received four reports of fires, smoke, and battery material ejection, though no injuries have been reported so far.

Serious·CPSC·Sep 3, 2026

These wooden dressers can tip over and trap children if not securely anchored to the wall. The dressers do not meet federal safety standards for clothing storage furniture. No injuries have been reported.

Serious·CPSC·Sep 3, 2026

GE is recalling four Portrait Core Services software products because a software issue may cause a loss of patient monitoring at the Hub and Central Viewer. After the update, alarm settings may also reset to factory defaults and no longer match the settings configured for each patient or care area. No injuries have been reported.

Serious·FDA·Sep 2, 20264 products

Olympus Corporation of the Americas is recalling POWERSEAL 5mm curved jaw sealer and divider devices due to incorrect labeling on the outer box. Some units labeled as 37 cm devices actually contain 23 cm devices, which could lead to confusion during surgical use. The issue affects 335 units distributed in the US, Australia, the European Union, and Japan.

Moderate·FDA·Sep 2, 2026

IMRIS is recalling 2 operating room table models, the ORT200 and ORT300, with 19 affected units. A mechanical failure in the linear actuator and rotational lock can stop the table from switching between locked and unlocked, which could allow unintended rotation during a procedure. No injuries have been reported.

Serious·FDA·Sep 2, 2026·IMRIS2 products

Healthmark Industries is recalling two ProChek protein test products, 5,143 units in total. The tests were made with an expired ingredient, so they may give false negative or false positive results. No injuries have been reported.

Moderate·FDA·Sep 2, 2026·Healthmark Industries2 products

FUJIFILM Synapse PACS software version 7.4.310, used in radiological imaging systems, has a software issue that can cause the ruler measurement tool to display inaccurate values. This affects 6 units distributed across select US states and Australia. No injuries have been reported.

Moderate·FDA·Sep 2, 2026·Fujifilm

Medline is recalling 11 groups of surgical convenience kits. The kits contain a component that the manufacturer recalled because it may be contaminated. No injuries have been reported, and the kits were distributed in 18 states.

Moderate·FDA·Sep 2, 202611 products

Some ConMed Linvatec GENESYS CrossFT Suture Anchors (REF# CFBC-5502B, Lot 1513167) may contain an incorrect patient implant card. This card is used to identify and track the device after implantation, so an incorrect card could lead to confusion about which device was used.

Moderate·FDA·Sep 2, 2026·ConMed

Fresenius Medical Care has identified a problem with certain 2008T BlueStar hemodialysis machines that can cause flow, water supply, or temperature alarms to malfunction. These alarms are important safety features that alert clinical staff to problems during treatment. About 1,140 affected machines have been identified by serial number.

Moderate·FDA·Sep 2, 2026