All Recalls

Honda is recalling 2018-2020 Odyssey vehicles because water intrusion can cause the rearview camera to fail, increasing the risk of a crash.

BMW is recalling various 2023-2025 BMW, Mini, and Rolls-Royce vehicles due to an integrated brake system malfunction that increases crash risk.

Chrysler is recalling Mopar headlights that may flicker or fail, reducing vehicle visibility and violating federal safety standards.

Chrysler is recalling 2026 Ram 1500 vehicles due to headlight wiring issues that may cause parking and daytime running lights to fail.

Honda is recalling 2026 Pilot and Passport vehicles due to improperly tightened rear subframe bolts that may cause stability loss.

Accord Healthcare is recalling 300 mcg Levothyroxine Sodium Tablets due to subpotency.

Lupin Pharmaceuticals is recalling three sizes of prednisoLONE Acetate Ophthalmic Suspension 1% due to the presence of a foreign substance.

Remel is recalling GC Agar Base plates due to a risk of reduced or no recovery of Neisseria gonorrhoeae strains.

Jayco is recalling 2027 Entegra Accolade and Jayco Seneca motorhomes because missing dinette brackets may cause the seating to detach.

Teko is recalling 2026 Triumph, Turbo, and Trophy vehicles because a missing alert system prevents them from making required pedestrian sounds.

Nissan is recalling JATCO automatic transmission control valve assemblies that may fail to correctly display the selected gear.

Ford is recalling certain 2024-2027 Lincoln Nautilus Hybrid and 2025-2027 Explorer Hybrid vehicles due to a missing pedestrian warning sound.

Ford is recalling 2024–2026 Mustang and 2025–2026 Mustang GTD vehicles because cold weather can cause windshield wiper and washer malfunctions.

Ford is recalling 2021-2023 Mustang Mach-E vehicles due to a risk of rear differential pinion shaft fracture and potential loss of drive power.

Nissan is recalling 2026 Rogue vehicles because the instrument panel may fail to display the gear selection, increasing the risk of a crash.

Chrysler is recalling 2026 Jeep Grand Wagoneer and Grand Wagoneer L vehicles due to a software error that may cause a loss of brake assist.

Chrysler is recalling certain 2022-2024 Jeep Grand Cherokee and Wagoneer vehicles due to a software error affecting the gear selection indicator.

Accord BioPharma is recalling Imuldosa (ustekinumab-srlf) 130 mg/26 mL injection vials due to a lack of assurance of sterility.

Le Chef Bakery recalls Mini Tiramisu and Mini Italian Pastry Assortment for undeclared Yellow #5.

Medline recalls arterial access kits with Huons lidocaine ampules over quality issues.

Medacta is recalling Short Monobloc Stem Broaches for the Shoulder System due to a risk of humerus fracture during surgery.

Tiffin is recalling various 2026-2027 recreational vehicles equipped with MaxxAir N-Series rooftop fans due to an overheating fire risk.

Jayco is recalling 2024 Alante and Entegra Vision RVs due to incorrect weight labels that may lead to vehicle overloading.

Medline recalls convenience kits with Swan-Ganz catheters over leak/breakage risk.

Diamond Coach is recalling 2025-2026 VIP motorcoaches with QRT-360 wheelchair retractors that may fail to lock, increasing injury risk.

Nissan is recalling 2025 Sentra vehicles due to a potential driveshaft installation issue that may cause power loss or vehicle rollaway.

Altec is recalling 2023-2025 Digger Derrick vehicles due to an incorrect pole rack capacity rating that may increase the risk of a crash.

Daimler Trucks is recalling 2026-2027 Thomas Built Saf-T-Liner HDX2 buses because the entrance door may fail to open or close.

Daimler is recalling 2026-2027 Thomas Built SAF-T-LINER HDX2 and EFX2 school buses because the entrance door may fail to open or close.

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

Boston Scientific recalls Intera 3000 pump over drug pathway leakage risk.

Medline recalls convenience kits with 10mL syringes over 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 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.