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

PAI Holdings LLC recalls VistaPharm, KERR INSTA-CHAR IN AN SORBITOL BASE WITH CHERRY FLAVOR, 50 Grams Activated Charcoal in 52 Grams Sorbitol in

VistaPharm recalls cherry-flavored activated charcoal in sorbitol base due to failure to meet OTC monograph standards. Consumers should check product details and contact the manufacturer for guidance.

PAI Holdings LLC recalls VistaPharm, KERR INSTA-CHAR IN AN AQUEOUS BASE WITH CHERRY FLAVOR, 25 Grams Activated Charcoal in 120 ml (4 fl oz),

PAI Holdings LLC recalls VistaPharm, KERR INSTA-CHAR IN AN SORBITOL BASE WITH CHERRY FLAVOR, 25 Grams Activated Charcoal in 26 Grams Sorbitol in

VistaPharm recalls cherry-flavored activated charcoal in sorbitol base due to failing to meet OTC monograph standards. This product may not be safe for use as intended.

CADILLAC ESCALADE (2025) recall — Wheels

Asclemed USA Inc. recalls Duloxetine DR Capsules, 30 mg, 30 count bottles, Rx, Relabeled by: Enovachem Pharmaceuticals, Torrance, CA 90501, NDC

Asclemed USA recalls 30mg Duloxetine DR Capsules due to nitrosamine impurity exceeding FDA limits. Consumers should check product labels for NDC 76420-634-30 and lot numbers 050725F-30 or 050725G-30.

Fresenius Kabi USA, LLC recalls Epinephrine Injection, USP, 1mg/mL, 1 mL single-dose vial, Rx only, Fresenius Kabi, Lake Zurich, IL 60047, NDC

Fresenius Kabi recalls specific batches of Epinephrine Injection due to failed impurities and degradations. Affected units may pose health risks if used improperly. Contact for details.