New York recalls

Food to Live Organic SuperGrass Powder in 6 oz, 12 oz, 1 lb, and 4 lb containers has been recalled due to Salmonella contamination. The affected products were distributed across the United States and U.S. Virgin Islands. No illnesses have been reported.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

A software update to GE's Portrait Core Services Software v1.0.5 may cause patient monitoring to stop working at the Hub and Central Viewer. The update can also reset all alarm settings back to factory defaults, overriding any custom alarm configurations set up for individual patients or care areas.

A software update to GE's Portrait Compute and Core Services system may cause patient monitoring to stop working at the Hub and Central Viewer. The update can also reset all alarm settings back to factory defaults, overriding the alarm configurations that were previously set up for individual patients or care areas.

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.

IMRIS Imaging Inc has recalled certain ORT300 operating room tables because the rotational lock mechanism may fail mechanically, preventing the table from locking or unlocking as intended. This could allow unintended movement during surgery, potentially injuring a patient. The recall affects 13 units with specific serial numbers.

A mechanical failure in the linear actuator and rotational lock mechanism on certain IMRIS ORT200 operating room tables may prevent the table from locking or unlocking properly. If the table becomes unlocked unintentionally during surgery, it could move unexpectedly and injure the patient.

Medline has recalled four models of surgical convenience kits used in neurosurgery procedures because they contain a component that may be contaminated. The affected kits were distributed nationwide to healthcare facilities in 18 states.

Medline Industries recalled four surgical convenience kits because they contain a component that may be contaminated. The affected kits are used in minor lithotomy, major lithotomy, gynecological laparotomy, and universal gynecological procedures. A total of 419 kits were distributed nationwide.

Medline Industries recalled three C-Section surgical convenience kits because they contain a potentially contaminated component from a supplier. The affected kits were distributed nationwide across 18 states. No injuries have been reported.

Medline Industries recalled 14 types of surgical convenience kits used in hospitals and surgical centers because they contain a potentially contaminated component that was recalled by the component manufacturer. The kits are used for various surgical procedures including gynecology, cardiac, thoracic, and transplant operations. No injuries have been reported.

Medline Industries has recalled certain convenience kits (model LTP CDS-LF, SKU CDS980375M, lot 25JBE079) because they contain a component that may be contaminated. The recall affects 15 kits distributed nationwide.

Medline Industries is recalling four types of surgical convenience kits because they contain a potentially contaminated component supplied by a manufacturer. The recalled kits were distributed nationwide to medical facilities. No injuries have been reported.