Medical DeviceJan 6, 2021
Lidco CM 50-001-01 Injectate Kit, accessory device to LiDCOunity v2 Monitor - Product Usage recall — FDA Z-0756-2021
The expiration date on labeling is incorrect.
Class IIFDA: TerminatedLidco Ltd
Recall history in this database
Classification mix: Class II: 1.
Understanding this recall history
This page summarizes recall records in which the official source identifies Lidco Ltd as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.