News - Pill Pals® - The Express Pharmacy

Update on Alert: Infusion Pump Software Issue from Fresenius Kabi USA

by Pill Pals | Mar 5, 2025 | News

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program. This recall involves correcting certain devices and does not involve removing them from where they are used or sold. The FDA has identified this recall as the most...

Update on Alert: Endoscope Accessories Issue from Olympus

by Pill Pals | Mar 5, 2025 | News

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program. This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause...

Update on Alert: Fluid Delivery Set Issue from Medline

by Pill Pals | Mar 5, 2025 | News

99000069FDS, 135, CHMN, W/F, MLL, RC(2), PG0000128741101934890695873019348906958199000069FDS, 135, CHMN, W/F, MLL, RC(2), PG0000134505101934890695873019348906958199000069FDS, 135, CHMN, W/F, MLL, RC(2), PG0000133893101934890695873019348906958199000069FDS, 135, CHMN,...

Update on Alert: Infusion Pump Issue from Fresenius Kabi USA

by Pill Pals | Mar 5, 2025 | News

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program. This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause...

January – March 2020 | Potential Signals of Serious Risks/New Safety

by Pill Pals | Mar 5, 2025 | News

Bridion (sugammadex) injectionArteriospasm coronary (coronary vasospasm) The “Adverse Reactions” section of the labeling was updated in January 2021 to include coronary spasm.Bridion labeling Bydureon (exenatide)Bydureon BCise (exenatide)Byetta...

Update on Alert: Nephroscope Sheath Issue from Trokamed GmbH

by Pill Pals | Mar 5, 2025 | News

This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program. This recall involves updating instructions for using certain devices, and does not involve removing them from where they are used or sold. The FDA has identified this...