794 recalls tagged with “infant product”.
Medline Unna-Z Stretch Zinc Paste Bandage faces a high-risk labeling error. The recall covers 35,328 units distributed in the U.S. and other regions. Manufacturers warn to stop use immediately and follow recall instructions.
Greatale recalled self-feeding pillows on January 15, 2026, due to a serious risk of aspiration and suffocation in infants. The pillows can hold a bottle at an unsafe angle, preventing infants from pulling away. Consumers must stop using the pillows immediately and return them for a full refund.
Yixing Trading recalled KEAWIS crib mattresses on January 15, 2026. The mattresses pose a suffocation and entrapment hazard due to improper fit in cribs. Consumers should stop using the mattresses immediately and seek a refund.
Aesculap recalls 126 MINOP TROCAR 150MM devices distributed nationwide to U.S. hospitals and clinics after regulators flagged a shaft length issue. The shaft may be longer than specified, potentially harming tissue during procedures. Healthcare facilities should stop using the devices and follow manufacturer recall instructions immediately.
Waldemar Link GmbH & Co. KG recalls 4 Endo-Model Replacement Plateau units worldwide, including the US state of New Jersey. A longitudinal fracture can detach the bushing from the screw shaft. Stop using the device and follow the manufacturer’s recall instructions.
Teva Pharmaceuticals USA, Inc. recalls 21,984 packages of Isotretinoin Capsules, USP, 30 mg. The lots are distributed to Florida, Ohio, Puerto Rico and Mississippi. The recall is active as of April 15, 2026.
Waldemar Link GmbH & Co. KG recalls its Endo-Model Replacement Plateau implant. Three units are affected worldwide, including New Jersey in the United States. The defect allows a bushing to detach from the screw shaft after a longitudinal fracture. Healthcare providers and patients should stop using the device immediately and follow the manufacturer’s recall instructions. Notification was sent by,
Teva Pharmaceuticals USA, Inc. recalls 8,376 isotretinoin 40 mg capsules distributed to FL, OH, PR and MS after FDA enforcement report flags superpotent and subpotent lots. Patients should stop use and contact their healthcare providers for guidance.
Waldemar Link GmbH & Co. KG recalls 8 units of Endo-Model Replacement Plateau worldwide after a reported risk that a bushing could detach from the screw shaft due to a longitudinal fracture. The recall also covers US distribution in New Jersey. Health authorities have classified the risk as high. Patients and healthcare providers should stop using the device immediately and follow recall guidance.
Kori Gey recalled water elf toy kits on January 8, 2026, due to a severe risk of battery ingestion. The toy kits can expose children to dangerous button cell batteries. Consumers should stop using the kits immediately and seek a refund.
Vasicar recalled 18,000 dressers on January 8, 2026, due to tip-over risks. The dressers can cause serious injury or death if not anchored to the wall. Consumers should stop using them immediately and seek a refund.
Lterfear recalled the Multifunction Pounding Game model D888 on January 8, 2026. The toy poses a serious ingestion hazard due to high-powered magnets that can detach. Consumers should stop using the toy immediately and seek a refund.
Infant Innovations recalled BabyBond retractable safety gates on January 8, 2026, due to a risk of serious injury or death from entrapment. The gates can allow a child's torso to fit through an opening, violating safety standards. Consumers should stop using the gates immediately and seek a refund.
Joyful Journeys recalled baby loungers on January 8, 2026, due to serious injury risks. The loungers pose fall and entrapment hazards to infants. Consumers should stop using them immediately and seek a refund.
Kalencom Corporation recalled SARO Braided Crib Bumpers on January 8, 2026, due to suffocation risks. The bumpers can obstruct an infant's breathing, violating federal safety regulations. Consumers should stop using the product immediately and seek a refund.
NFSVLB recalled baby bath seats on January 8, 2026, due to a drowning hazard. The recall affects the model number ZY2025, which can tip over and entrap children. Consumers must stop using the seats immediately and seek a refund.
Olympus Corp. of the Americas recalls 55 ShockPulse-SE Lithotripsy System units distributed internationally. Mis-wired component may create noise on the power supply and ultrasonic circuit. Hospitals and providers should stop using the device immediately and follow recall instructions. Notify Olympus or your healthcare provider for guidance.
Raz Design Inc recalled 66 Raz Mobile Shower Commode Chairs nationwide, citing a modification that may allow the seat to detach if outside rear brackets are not properly engaged. The recall covers multiple catalog numbers and serial ranges. Patients and healthcare providers should stop using the device immediately and contact Raz Design for instructions.
Toyota recalls 2021-2025 Sienna Hybrid vehicles for third-row seatback bolts that may not be tightened. The unsecured bolts may fail to restrain occupants in a crash. Owners should contact their Toyota dealer for inspection and service; recall number 25TA05; letters were mailed April 1, 2025.
Cipla USA, Inc. is recalling 15,221 Lanreotide Acetate Injection syringes nationwide in the United States after detecting particulate matter. The defect is the presence of particulate matter in the injectable solution. Healthcare providers and patients should stop using the product immediately and contact Cipla USA for guidance.