Medline issues correction for convenience kits containing recalled ICU Medical pain management components
Medline announced a correction for certain convenience kits that include ICU Medical pain management components containing Huons Bupivacaine Hydrochloride in Dextrose Injection.
The FDA classified this recall as the most serious type because the device could cause serious injury or death if used without correction. Medline is advising customers to remove the affected components before further use.
The correction does not require removal of the kits from use or sale; instead, customers should follow Medline's letter to correct the kits. A list of affected product SKUs and lot numbers is provided.
This writeup was produced by pharmadog from original reporting by fda medwatch.
Original headline: “Convenience Kit Correction: Medline Issues Correction for Convenience Kits Containing ICU Medical Pain Management Components”
read at fda medwatch ↗
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