United StatesThe Aligned Medical AMS16835 Fluids Kit RX custom convenience kits (UDI‑DI B098AMS168350; lot numbers 233828, 236048, 236359, 236662, 238580, 239934, 239935) — 875 kits distributed in Illinois and Virginia — are affected. They were recalled because Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for quality issues, was included in the kits.
What's being recalled
Aligned Medical AMS16835 Fluids Kit RX
Recalling firm: Windstone Medical Packaging, Inc., Billings, MT, United States.
How to identify it
UDI-DI: B098AMS168350; Lot Numbers: 233828, 236048, 236359, 236662, 238580, 239934, 239935
The hazard
Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for quality issues, was included in custom convenience kits.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Nationwide distribution in the states of IL, VA.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)