All Recalls

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 over incorrect tubing assembly.

Surgify Halo 3.0 mm Extendable drill recalled over burr breakage risk 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 Shoulder Reamer Guide Model 110040240 due to breakage risk.

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 assembly issue causing cable pull-out and loss of speaker output.

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.

Mars Snacking recalls MorningStar Farms Buffalo Chik'n Nuggets and Sausage Patties over 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 from 7 brands over defective container seals.

HeartMate 3 LVAS kits recalled due to backup battery failures.

International Food Products recalls 3 dairy powder products in 50 lb bags due to Salmonella.

United Salt recalls salt products due to mislabeling of iodized and plain varieties.

Staar Surgical is recalling Version 8.00 of its ICL Calculation Software due to a coding error affecting toric lens orientation diagrams.

Inspire Medical recalls Respiratory Sensing Lead Model 4340 due to incorrect Use By dates that may cause premature revision surgery.

Abiomed is recalling Impella CP Sets with SmartAssist due to a risk of low purge pressure that may interrupt mechanical circulatory support.

BD is recalling Connecta Luer-Lok stopcocks due to a potential connection failure at Port C when using plastic luer-lok syringes.

Merit Medical is recalling various Splashwire Hydrophilic Guide Wire models due to unsealed pouches that may compromise device sterility.

Piaggio is recalling 2026 Liberty 50 and 150 motorcycles due to an electrical fault that may cause the headlights to unexpectedly turn off.

Toyota is recalling 2026 Toyota BZ, Lexus RZ, and Subaru Solterra EVs due to an ECU fault that may cause a loss of drive power.

Farber Specialty is recalling 2025-2026 emergency vehicles because the touchscreen may fail, disabling emergency lights and equipment.

GM is recalling 2026-2027 Cadillac Vistiq vehicles because the third-row power seatback may fail to reverse, posing an entrapment risk.

Par Health is recalling Buprenorphine HCl Injection due to crystallization identified as Buprenorphine free base.

Stryker recalls Triathlon Universal Baseplate due to packaging mix-up between Size 3 and Size 4.