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

King Systems Corp. dba Ambu, Inc. recalls KING LTSD,SIZE 2,W/SUCTION PORT STERILE-Inserted into a patient s pharynx through the mouth to provide patent airway.

Ambu recalls KING LTSD Size 2 airway devices for pediatric use risks. Devices may cause harm if used beyond intended medical applications.

Integra LifeSciences Corp. recalls Duraform Dural Graft Implant, Size 3x3 , Model Number 80-1477US Lot CT007694

Integra LifeSciences recalls specific Duraform Dural Graft Implant (Model 80-147: Lot CT007694) due to potential endotoxin levels outside specifications. Affected patients should contact for guidance.

BUICK ENVISION (2024) recall — Equipment

Fresenius Kabi Compounding, LLC recalls Phenylephrine HCl 0.9% Sodium Chloride Injection USP, 10 mg per 250 mL, Single Dose Bag, Rx only, Fagron Sterile

Fresenius Kabi recalls phenylephrine injection due to cGMP violations. Affected units have specific lot numbers and expiration dates. Consumers should contact the manufacturer for details.

Fresenius Kabi Compounding, LLC recalls Phenylephrine HCl 0.9% Sodium Chloride Injection USP, 20 mg per 250 mL, Single Dose Bag, Rx only, Fagron Sterile

Fresenius Kabi recalls phenylephrine injection due to CGMP violations. Affected lots may have safety issues; check NDC and expiration date for details.