Voluntary nationwide recall: Eye drops (Leader)
Nov. 2023Pharmacy Updates
Cardinal Heath Inc. has recalled certain lots of Leader brand eye drops. These over-the-counter products are used for temporary relief of burning, irritation, and redness of the eye. The drops are being recalled because of bacteria found in certain samples of the product. The bacteria could cause eye infections that result in partial vision loss or blindness. Read the full text of the Leader brand eye drops recall.
Recent Announcements
CME Webinar: The State of Telehealth in 2026
Please join us for a live, CME-accredited webinar on Tuesday, Jan. 27, from noon to 1 p.m. that will share updates on the state of telehealth for 2026.Dec. 2025Education/Webinars
Formulary updates effective Jan. 1, 2026
Review upcoming policy and operational updatesDec. 2025Pharmacy Updates
Voluntary nationwide recall: Famotidine (Fresenius – November)
Fresenius Kabi USA, LLC is recalling three lots (6133156, 6133194, and 6133388) of Famotidine Injection, USP, 20 mg per 2 mL. Famotidine is used to treat excessive secretion of stomach acid or stomach ulcers.Nov. 2025Pharmacy Updates