
NHTSA•MODERATE
Ford Mustang Mach-E Rear Differential Pinion Shaft
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.

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.
2 products
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.

Medline recalls 3 convenience kits with Huons Lidocaine ampules due to quality issues.
19 products
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.
2 products
Jayco is recalling 2024 Alante and Entegra Vision RVs due to incorrect weight labels that may lead to vehicle overloading.

TNVitamins Organic Moringa Capsules and Powder recalled due to possible Salmonella contamination.

Medline recalls convenience kits with BD Swan-Ganz catheters due to hub failure risk.
9 products
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.

High Valley Orchard Chocolate Covered Raisins recalled over undeclared peanut allergen.
2 products
Treatlife smoke and CO detectors are recalled because they may fail to alert users to a fire, posing a risk of injury or death.

Amana air conditioners and heat pumps are recalled due to a fire and burn hazard caused by a faulty heating element.

Honlyne LED party favors (Model HON-302HE) are recalled due to a button cell battery ingestion hazard that can cause serious injury or death.

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.
23 products
Abiomed recalls Impella CP introducer kit (14 Fr x 13 cm) over thrombus risk.
4 products
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.
2 products
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.

Medline recalls CV Anesthesia Room Setup kits due to quality issues with included lidocaine and bupivacaine injections.
5 products
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.
3 products
Surgify Halo 3.0 mm burr recalled due to potential breakage during spinal surgery.
19 products
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.
2 products
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.
2 products
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.
2 products
Amgen recalls Corlanor and Sensipar tablets over foreign substance contamination.
5 products
Zimmer recalls Off-Axis Reamer Guide (Model 110040240) due to breakage risk from catching during reaming.
5 products
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.
