Know if it’s recalled — and exactly what to do.

HYUNDAI PALISADE (2026) recall — Seats

FORD MAVERICK (2026) recall — Visibility

FORD F-53 (2025) recall — Exterior Lighting

Straumann USA LLC recalls Custom Abutment AS Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 010.5438;

Straumann recalls Custom Abutment AS Ti for Straumann RC with TAN screw due to manufacturing mix-up using incorrect material. Affected units have specific catalog numbers and order numbers.

Straumann USA LLC recalls Custom Abutment Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 027.4620;

Straumann recalls Custom Abutment Ti products (Catalog 027.4620) due to manufacturing error using incorrect material. Affected items may have safety risks.

Chiesi USA, Inc. recalls CUROSURF (poractant alfa), 240 mg, Intratracheal Suspension, 3L Single-dose-Vial, Rx only, Chiesi USA, Inc, Cary, NC

Chiesi USA recalls CUROSURF 240mg intratracheal suspension vials due to lack of sterility assurance. Affected lots expire 09/2026 and 10/2026. Contact for remedy details.

Teva Pharmaceuticals USA, Inc recalls Octreotide Acetate for Injectable Suspension, for gluteal intramuscular use, 30 mg, Single-dose 8 mL vial in Kit, Rx

Teva Pharmaceuticals recalls Octreotide Acetate vials for gluteal use due to potential sterility issues from manufacturing quality failures. Affected lots expire through 2027.