
NHTSA•MODERATE
Ricon R1200 Power Transfer Seat Base
Ricon is recalling R1200 series Power Transfer Seat Base units over potential gear motor locking failure.

Ricon is recalling R1200 series Power Transfer Seat Base units over potential gear motor locking failure.

Ford is recalling 2026 Explorer and Mustang vehicles for incorrectly installed piston circlips that may cause engine failure and loss of drive power.

Nova Bus is recalling 2025 and 2024 LFS Artic transit buses; window glass may detach due to inadequate frame adhesion.

Toyota is recalling 2023–2025 Corolla Cross Hybrid vehicles for insufficient pedestrian warning sounds in reverse.

Ford is recalling 2025–2026 Bronco Sport and Maverick vehicles; front passenger air bag may not deploy due to OCS sensor failure.

Ford is recalling 2021–2023 Lincoln Navigator, Expedition, and 2022–2023 F-Series Super Duty trucks due to windshield wiper arm breakage.

Ford is recalling 2026 Lincoln Aviator and Explorer vehicles for HVAC system failure affecting windshield defrosting.

Amneal is recalling 500-count bottles of Tramadol Hydrochloride 50 mg tablets due to an impurity found during stability testing.

Chiesi USA is recalling Curosurf 240 mg intratracheal suspension vials (NDC 10122-510-03) due to lack of sterility assurance.

Synthes recalls VOLT Locking and Cortical Screw Taps due to incorrect thread from a lot swap.
2 products
Olympus recalls SOLTIVE laser systems (TFL-SLS, TFL-PLS) due to power supply defect that may cause inoperability and smoke.
2 products
Aston Martin is recalling 2021–2026 DBX models due to rear suspension arm pin failure risking loss of control.

Terex is recalling pole guide arm assembly pins (part 450543) due to cracked welds that may cause the arm to fall.

Vital Nutrients Aller-C is recalled due to undeclared egg, soy, and hazelnut allergens.

Teva recalls Octreotide Acetate 20 mg vials over sterility assurance concerns.
6 products
A recall was issued for Artoura Breast Tissue Expanders due to infusion sets that may contain dull or blunt needle tips.
7 products
Philips recalls Allura Xper FD10/FD20 systems over wired foot switch failure causing intermittent X-ray imaging.
22 products
Medline recalls ENFit G-tube connectors in care/discharge kits over seal failure and leakage risk.
2 products
Waldemar Link recalls Embrace Drill Tower instruments over mixed-up article numbers in the surgical technique overview.
2 products
Ultradent is recalling Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011, due to crumbling and breakage risk.

Medline is recalling Sterile Radiology Procedure Kits Model DYNDH1491B due to potential sterile pouch packaging breach.

Stryker is recalling the CHROMOPHARE Softlit Ring Surgical Light System due to a potential ceiling cover support failure.

ReCor Medical is recalling the Paradise Ultrasound Renal Denervation Catheter (Model PRDS-068-02) as these units were intended to be scrapped.
3 products
Philips Vue Motion V12 (1017979) may display image frames out of sequence during dynamic imaging runs.

Medline is recalling Puracol and Puracol Plus wound dressings due to elevated endotoxin levels that may cause severe inflammatory responses.

Luxfer is recalling gas cylinder adapters (model EP-O-350-8-U5) due to O-ring incompatibility risking hydrogen leak and fire.
2 products
Mercedes-Benz is recalling 2025 G580 vehicles with incorrect wheel bolts that may loosen or detach.

Mercedes-Benz is recalling 2026 GLE and GLS models over passenger air bag fabric defect that may prevent deployment.

KTM is recalling 2022–2024 390 Duke and RC 390 motorcycles due to throttle control unit water ingress causing loss of power.

Triumph is recalling 2026 Trident 800 motorcycles with improper headlight low beam illumination that increases crash risk.

Siemens is recalling the Atellica CH A1c_E assay due to a risk of depressed results when used alongside the RCRP assay on the same analyzer.

American Laboratories recalls pepsin powders (Full Strength, 1:10,000, 1:3000) due to potential Salmonella contamination.
3 products
Lucid is recalling 2024–2026 Air Pure RWD vehicles over half-shaft disconnection risk due to loose bolts.

Gillig is recalling 2023–2024 Low Floor transit buses with Michelin X InCity Grip D tires due to GAWR placard exceeding tire load rating.

Chrysler is recalling 2022–2026 Pacifica and Voyager vehicles for defective side curtain air bags that may fail to prevent ejection in a crash.

ABC BUS is recalling Van Hool buses (C2045, T2145, TX45, CX45, CX35) with incorrect door window glaze that may reduce visibility.

Honda is recalling 2025 CB1000SP motorcycles due to fuel hose disconnection risk and potential fuel leak.
Chrysler is recalling Mopar side curtain air bags (part numbers 68224526AJ, 68224527AH) over insufficient pressure retention from sealed seams.

Lucid is recalling 2025–2026 Gravity vehicles for defective second-row seat belt anchor brackets that may fail in a crash.
2 products
BD Alaris System labeling lacks required TLS version specification for secure Wi-Fi communication with Point-of-Care Units.

FSIS alert: Blackwing Organic Meats beef and pork products made without inspection may contain undeclared allergens or bacteria.
8 products
Apotex is recalling Brimonidine Tartrate/Timolol Maleate eye drops (NDC 60505-0589-1) due to lack of sterility assurance.

Olympus recalls PKS Cutting Forceps over jaw breakage risk from defective welds.
7 products
Howmedica Osteonics is recalling the MICS3 Angled Sagittal Saw Attachment due to a risk of external screws loosening and detaching during use.

Volvo is recalling 2025–2026 VNL (4) trucks over delayed brake release that increases crash risk.

Volvo Trucks is recalling 2025–2026 VNL (4) vehicles for instrument panel display failure that may hide speedometer and warning lights.

Volkswagen is recalling 2025 Jetta and Taos vehicles with instrument panels that may fail to display warning lights or gauges.

Aston Martin is recalling 2025–2026 DBX and 2026 DBX S vehicles; TPMS warning light may not illuminate for low tire pressure.

South Florida Food recalling Pan de Bono Cheese Bread (14.4 lb boxes) due to undeclared soy.

Macleods Pharma recalls Levothyroxine Sodium 150 mcg tablets (NDC 33342-401-44) nationwide due to subpotency.
