New York recalls

Love To Dream portable sleep machines contain a lithium-ion battery that can overheat if an incompatible charger is used. This overheating poses a risk of fire or burns.

The left temple of INMO Air3 Smart Glasses can overheat during extended use, causing burns to the face and ear. The company has received 10 reports of overheating, including burning sensations. The affected glasses were sold online between December 2025 and August 2026.

Style Homeware Emerspring mattresses sold on Amazon do not meet federal flammability standards for mattresses. This poses a risk of serious injury or death if a fire occurs near the mattress.

These wooden dressers can tip over and trap children if not anchored to the wall. The dressers do not meet federal safety standards for furniture stability. One tip-over incident has been reported, though no injuries have occurred.

Xinan Home WinxMatrs twin-size mattresses do not meet federal flammability standards and pose a risk of serious injury or death from fire. The black, 10-inch-thick mattresses were sold compressed in boxes on Amazon from August through November 2025.

NEWDERY power banks with model number ZHX-PB22 (black with yellow cables) can have lithium-ion batteries that unexpectedly explode or catch fire. The company has received nine reports of fires, including one that caused $2 million in property damage and one burn injury.

The lithium-ion battery packs in Blue Cactus Company Reclining Chair model RWX-RBP02 can overheat and catch fire or cause burns. About 51,000 units were sold on Amazon between May 2023 and July 2026. The company has received four reports of batteries overheating, smoking, or igniting.

5Color size-small bicycle helmets in children's helmet and pads sets do not meet mandatory federal safety standards. The helmets may fail to protect a child's head in a crash, creating a serious risk of injury.

Kesyup-branded mattresses sold on Amazon do not meet mandatory U.S. flammability standards for mattresses. The mattresses are 12 inches thick, available in twin, full, queen, and king sizes, and have a white top with blue sides and trim. They were sold in compressed boxes from December 2024 through April 2026.

Berlin Seeds is recalling 950 pounds of alfalfa sprouting seed sold from February to August 2026 because it may be contaminated with Shiga toxin-producing E. coli (STEC) and/or Salmonella. The contamination was identified after a sprout grower using this seed was linked to a multistate outbreak investigation. One illness has been reported.

Pi-Cardia Inc. identified a weld issue in the ShortCut transfemoral catheter that may cause the positioning arm to detach during use. The defect affects 46 units in specific serial number lots distributed across eight U.S. states. No injuries have been reported to date.

ICU Medical's CADD Yellow Medication Cassette Reservoirs may leak medication at the connection point between the luer connector and tubing. This leakage could delay or stop medication delivery, reduce the amount of medication received, expose patients to contamination, or allow air to enter the bloodstream.

Reign Medical's Clench Staple System (Compression) was distributed without adequate performance testing and requires additional FDA clearance. The device is used in bone fixation procedures. About 600 units were distributed nationwide.

Some Medline Cataract Pack convenience kits (model DYNJ59881A, Lot 25GBP246) may have open seals in their sterile pouch packaging. An open seal can allow the sterile contents to become contaminated. If a kit with an open seal is used without being detected first, it could introduce infection into the surgical field or patient.

Medline Industries' myringotomy convenience kits (model MYRINGOTOMY PACK-LF, lot 25FBU754) may have open seals in their sterile pouches. An open seal can allow contamination that may not be visible before use, potentially leading to infection if the kit is used on a patient.

Medline Industries convenience kits (model numbers DYNJ58421A and DYNJ40734F) may have open seals in their sterile pouch packaging. An open seal can allow bacteria or other contaminants to enter the package, potentially compromising the sterility of the product. If used without detecting the open seal, this could lead to infection or contamination during a medical procedure.

Medline Industries anesthesia pain relief convenience kits may have open seals in their sterile pouch packaging. An open seal can allow bacteria or other contaminants to enter the package, potentially compromising the sterility of the medical supplies inside. If used without noticing the damaged seal, these kits could introduce infection into the surgical field or patient.

Certain Scorpio + Mobile Bearing and System One Bipolar hip implant components were manufactured with polyethylene material that had aged beyond recommended limits. This aged material can develop excessive oxidation, leading to accelerated wear, material fragmentation, or device failure.

Howmedica Osteonics TRIDENT 0° poly insert knee implants (model 620-00-28D) were made with aged polyethylene material that can break down faster than intended. This may cause the implant to wear excessively, crack, or loosen inside the knee, potentially requiring revision surgery.

Howmedica Osteonics manufactured SCORPIO recessed metal-backed patella implants using polyethylene material that was stored longer than five years before use. This aged material can develop oxidation, which may cause the implant to wear faster than expected, potentially leading to device failure, fractures, or loosening.

Certain orthopaedic implant components (bearing and axle bushings, tibial inserts, and glenoid components) were manufactured with aged raw material that may have elevated oxidation levels. This can lead to increased wear, material fragments, or device fracture.

Howmedica Osteonics manufactured acetabular (hip socket) and other orthopaedic implant components using polyethylene material that was aged beyond recommended limits. This aging can cause oxidation and increased wear, potentially leading to device fracture, material breakdown, or component separation inside the body.

Certain Howmedica Osteonics shoulder implant components were made with aged polyethylene material that can develop excessive oxidation. This may cause the implant to wear faster than expected, potentially leading to device fracture or loosening, material fragments, and the need for revision surgery.

Howmedica Osteonics manufactured certain Triathlon Hinge Insert knee implant components using raw material that had aged more than five years, which can develop excessive oxidation. This may cause the implant to wear faster than expected, potentially leading to device fracture, material fragments, or loosening that could require revision surgery.

Howmedica Osteonics manufactured multiple knee implant components (inserts, bearings, and patella components) using polyethylene material that was stored for more than five years before use. The aged material may have developed excessive oxidation, which can cause the implant to wear faster than intended and potentially break apart inside the body.

Howmedica Osteonics recalled certain OMNIFIT Series I acetabular inserts (Catalog No. 2001-2246) because the polyethylene material used was aged beyond recommended limits. This aging can cause increased oxidation and premature wear, potentially leading to device fragments, fracture, or loosening inside the body.

Howmedica Osteonics manufactured certain elbow implant axle pins using aged polyethylene material that can develop excessive oxidation over time. This may cause the device to wear prematurely, crack, or break apart inside the body, potentially requiring revision surgery.

The tension bolt in certain Mirion Captus 4000e thyroid imaging systems can fail, allowing the spring arm to unexpectedly drop to its lowest position, about 25 inches from the ground. This affects specific models shipped between April 2019 and February 2024 that have not yet received the redesigned arm. No injuries have been reported.

Certain Datex-Ohmeda anesthesia delivery systems with electronic gas mixer assemblies can unexpectedly switch to a backup oxygen-only mode, which stops anesthetic agent delivery and requires immediate clinician action. If not addressed quickly, patients may receive less anesthesia than intended during surgery.

Certain Datex-Ohmeda Aisys CS2 anesthesia systems with specific electronic gas mixer assemblies can automatically switch to a backup oxygen-only mode. When this happens, the delivery of anesthetic medication stops, and the system triggers alarms. A clinician must manually intervene to restore anesthetic delivery, or the patient may not receive adequate anesthesia.