All Recalls

Kith is recalling children's loungewear sets due to a violation of federal flammability standards, posing a risk of serious burn injuries.

Small Fish Montessori Busy Board (model 2512JX02) is recalled due to a magnet ingestion hazard that can cause serious injury or death.

Raychy children's light-up sneakers are recalled due to a serious battery ingestion hazard from accessible lithium coin batteries.

Lomi Roll-On Waxing Kits are recalled because the warmer's power cord can overheat, posing fire, burn, and shock hazards.

Sunderwell XW-A17 youth electric ATVs are recalled for missing brake lights, which poses a crash hazard and violates federal safety standards.

Elevate Oral Care is recalling Povi-One 10% Povidone-Iodine Oral Antiseptic due to sub-potency.

Intera 3000 Hepatic Artery Infusion Pump recalled over potential drug pathway leakage.

Medline recalls convenience kits with 10mL polycarbonate syringes due to unapproved design changes.

Sun Pharmaceutical is recalling 6mg Perampanel CIII tablets due to a labeling mix-up where bottles may contain 10mg tablets.

Camber Pharmaceuticals is recalling Lacosamide 100mg tablets due to a potential mix-up with Selexipag 1000 mcg tablets.

ANI Pharmaceuticals is recalling Hydroxyzine Hydrochloride Oral Solution, 10 mg/5 mL, due to the presence of a foreign substance.

Philips is recalling Telemetry Monitor 5500 units due to a potential reset error that prevents connection to the central monitoring system.

IPG Medical is recalling the Thuvera Laser Console due to a software anomaly that may cause a false error code 5018 display.

GE Healthcare is recalling the AW Server 3.2 ext.6.5 image processing system due to a software error that may display the wrong patient's data.

Medtronic recalls Octopus Evolution Tissue Stabilizer TS2000 due to incorrect tubing assembly.

Surgify Halo 3.0 mm burr recalled due to potential breakage during spinal surgery.

Stryker is recalling the InZone Detachment System due to premature battery drain that may prevent coil detachment during medical procedures.

Airstream is recalling certain 2026 Classic trailers and 2025-2027 Interstate RVs due to a fire risk from overheating Maxxfan circuit boards.

Hyundai is recalling 2025-2026 Tucson vehicles due to a software error that may cause the instrument panel display to fail.

Ford is recalling 2022-2026 Bronco vehicles because improperly secured fender flares may detach, creating a road hazard.

Ford is recalling various 2018-2021 Ford and Lincoln vehicles due to a transmission park pawl issue that may cause a vehicle rollaway.

Harbinger is recalling 2025 Stripped Chassis vehicles due to steering gear bolts that may loosen or break, increasing the risk of a crash.

Elgin is recalling 2024-2026 Pelican vehicles with Samsung SDI high voltage battery packs due to a fire risk from potential battery failure.

Direct Rx is recalling 30 mg Duloxetine Delayed-Release capsules due to N-nitroso-duloxetine impurity levels exceeding FDA limits.

Acumed is recalling various hexalobe screws used in wrist fixation systems due to a risk of the screws breaking during use.

Amgen recalls Corlanor and Sensipar tablets over foreign substance contamination.

Zimmer recalls Off-Axis Reamer Guide (Model 110040240) due to breakage risk from catching during reaming.

PFM Medical is recalling Multi-Snare Set catheter devices due to a failure to meet biocompatibility requirements for in-vitro cytotoxicity.

Ventec is recalling the VOCSN+Pro respiratory system because a damaged battery may prevent the backup alarm from sounding during power loss.

GM is recalling 2025-2026 Express and Savana vehicles due to a steering gear assembly nut that may not be properly tightened.

Rockford is recalling four amplifier kit models due to a 150-amp fuse defect that poses a fire risk.

Ricon is recalling S-Series and K-Series wheelchair lifts because a faulty electrical contactor may cause the lift to move unexpectedly.

Major Pharmaceuticals is recalling 0.2 mg Methylergonovine Maleate Tablets due to subpotency.

Ajanta Pharma is recalling Fenofibrate Capsules, USP 200 mg, due to manufacturing process deviations.

Philips recalls Avalon Fetal Monitor FM20 over speaker connector issue that may cause loss of speaker output.

Boichik Bagels recalls Whitefish Salad, Tuna Salad, and Pumpernickel Mix Bagels over undeclared eggs.

Intuitive Surgical is recalling the Da Vinci surgical system E-brake retainer pin due to a risk of uncontrolled motion and patient injury.

TMJ Solutions is recalling custom temporomandibular joint implants due to incorrect components causing a poor fit and potential open bite.

Forest River is recalling 2025-2027 NOBO, Ibex, and RPOD trailers due to mislabeled 110V circuits that pose an electrical shock risk.

Airxcel is recalling MaxxAir N-Series Maxxfan rooftop ventilation fans due to a risk of fire from an overheating printed circuit board.

Indian Motorcycle is recalling 2026 Chief Vintage motorcycles due to an incorrect rear rim width listed on the VIN label.

MorningStar Farms recalls Buffalo Chik'n Nuggets and Hot & Spicy Sausage Patties over possible plastic contamination.

Arizer is recalling Solo III portable vaporizers due to fire and burn hazards affecting specific serial prefixes and UPC 628078802274.

BABESIDE doll and stroller sets are recalled due to a choking hazard from small parts that violate federal safety standards.

GOPO Toys is recalling pull string teething toys due to a serious choking hazard caused by strings that violate federal safety standards.

Joolz is recalling Aer2 car seat adapters because they can fail to attach to the stroller, posing a fall hazard to children.

CooCooBaby is recalling Classic and Deluxe baby loungers due to suffocation and fall hazards that violate federal infant sleep safety standards.

Michley children's pajamas are recalled for failing to meet federal flammability standards, posing a serious burn injury or death risk.

Veseacky children's pajama sets are recalled for violating federal safety standards, posing a serious burn injury or death risk to children.

Keystone recalls 20% benzocaine gels (Pearson, Quala, DHP, etc.) over defective seals.