I heard that Bausch and Lomb has issued a recall. I want to know the reason behind this recall. Is it due to some quality issues or safety concerns with their products? I'm curious to understand why they made this decision.
7
answers
Nicola
Sat Mar 01 2025
The affected devices are being removed from locations where they are used or sold.
Lorenzo
Sat Mar 01 2025
This recall is considered to be of the most serious type by the FDA.
Tommaso
Sat Mar 01 2025
Bausch + Lomb/Synergetics Inc. has initiated a recall of Eye Injection Kits.
Margherita
Sat Mar 01 2025
The FDA has classified this recall as a Class I recall, indicating a serious health hazard.
Tommaso
Sat Mar 01 2025
The reason for the recall is due to potential non-sterility of certain I-Pack Injection Kits.