New York recalls

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.

EAK Distribution recalled Home Grown Green Sprouting Calabrese Broccoli Seeds (8 oz, Heirloom) sold on Amazon between August 20 and September 18, 2026, because they may be contaminated with Salmonella. The contamination was discovered after the seed supplier identified the lot as potentially used in a sprout grower's product linked to a multistate foodborne illness outbreak.

Greenwich Rx, a compounding pharmacy, is recalling specific lots of compounded glutathione injection due to potential elevated endotoxin levels. Elevated endotoxins in injectable products can cause serious reactions including fever, low blood pressure, and in severe cases, anaphylactic shock or death. The affected product was distributed nationwide between June 26 and September 21, 2026.

Agrish adult portable bed rails (models AG-12011, AG-12014, AG-12016) do not meet safety standards and can trap users between the rail and mattress, creating a risk of serious injury or death. The rails also have structural problems that increase fall risk and sharp edges that can cause cuts.

Golden Resale's portable camping showers contain immersion heaters that can ignite when partially or completely out of water, creating a serious fire risk. About 400 units were sold online through Amazon and Walmart from February to August 2026. No injuries have been reported.

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.

Kobayashi rechargeable hand warmers contain lithium-ion batteries and electrical components that can overheat and ignite. This poses a risk of fire and serious burns to users.

Metal wire bristles can detach from Walmart Expert Grill brushes and stick to food or the grill surface. If swallowed, these bristles can cause serious internal injuries that may require surgery.

Gobi Heat rechargeable hand warmers (model UT3053) can overheat and catch fire due to a problem with the built-in lithium-ion battery and electrical components. The black hand warmers with gray accents were sold in pairs online from October 2024 through August 2026. No injuries have been reported, but the company is recalling them out of caution.

These magnetic stick figure toy sets contain high-powered magnets that can come loose and be swallowed by children. If ingested, multiple magnets can attract each other inside the digestive system, causing serious internal injuries including perforations, blockages, and in severe cases, death.

The cord or internal wiring in these floor lamps can overheat, smoke, spark, or catch fire when the lamp is plugged in or turned on. The company has received 11 reports of problems, including two incidents involving shock and burn injuries.

YunHeng's LandTale portable bed rails can trap users between the rail and mattress, creating a serious risk of asphyxiation. The rails also lack required warning labels. About 730 units were sold online through Amazon from February to June 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.

ABC Trading's squishy dumpling and crazy squib ball 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 internal injury.

Medline has recalled 28 models of surgical convenience kits used in spine and brain surgery. The kits contain neurological sponges with potentially elevated endotoxin levels — bacterial contamination that can cause fever, inflammation, low blood pressure, or other complications during or after surgery.

Medline Industries is recalling seven surgical convenience kits used in neurosurgery procedures. The neurological sponges in these kits may contain higher-than-expected endotoxin levels (bacterial toxins), which could cause adverse reactions during or after surgery.

Medline's Convenience Kits Major Pack (catalog number DYNJ81325A) contain neurological sponges with unexpectedly high levels of endotoxin, a bacterial byproduct. These elevated levels could trigger serious medical reactions including fever, inflammation, or low blood pressure that may require medical care.

Medline's surgical convenience kits contain neurological sponges with unexpectedly high endotoxin levels—a bacterial byproduct that can trigger serious reactions. The affected kits are used in sinus, nasal, and ENT procedures. Elevated endotoxin exposure may cause fever, inflammation, low blood pressure, or other reactions that need medical care.

Baxter Healthcare's PRO+ 40" MRS SURFACE mattress has an error in the product description printed on its UDI (Unique Device Identification) label. This mislabeling may cause healthcare facilities or users to misidentify the product or select an incompatible bed frame, potentially affecting safe use of the mattress.

Baxter Healthcare's PRO+ 36" MRS SURFACE mattress has an error in the product description on its Unique Device Identification (UDI) label. This mislabeling could cause the mattress to be confused with other products or used with an incompatible bed frame.

The Baxter PRO+ MRS SURFACE FOR VERSACARE mattress has an error in the product description on its UDI (Unique Device Identification) label. This labeling discrepancy may cause the product to be incorrectly identified or selected, which could result in the mattress being used with an incompatible bed frame.

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.

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.

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.

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.

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.

Cardinal Health Presource Convenience Kits contain applicators with potentially open or incomplete seals on their packaging. If a contaminated applicator is used, it could cause a localized skin or soft tissue infection, or in rare cases, a more serious systemic infection.

Cardinal Health Presource Convenience Kits contain applicators with packaging that may have an open or incomplete seal. If an applicator becomes contaminated, it could cause a localized skin or soft tissue infection, or in rare cases, a more serious infection.

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.

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.