United StatesMEDLINE STERILE BASIC EYE PACK 16 (REF DYNJ37743D, Lot 25EMI333, UDI/DI 10193489600124; REF DYNJ37743F, Lot 25GMD927, UDI/DI 10198459390685) is affected. The kits were recalled because specific sterile eye procedure kits with pouch packaging may exhibit open seals. These units were distributed in Missouri.
What's being recalled
MEDLINE STERILE BASIC EYE PACK 16: 1) REF: DYNJ37743D; 2) REF: DYNJ37743F.
Recalling firm: Medline Industries, LP, Northfield, IL, United States.
How to identify it
1) REF: DYNJ37743D: UDI/DI 10193489600124 (each), 40193489600125 (case), Lot Number 25EMI333; 2) REF: DYNJ37743F: UDI/DI 10198459390685 (each), 40198459390686 (case), Lot Number 25GMD927.
The hazard
Medline has identified specific sterile eye procedure kits with pouch packaging that may exhibit open seals.
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: MO
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)