Class II — Lidco Ltd
| Recalling firm | LIDCO LTD. |
|---|---|
| Registered facility | LIDCO LTD. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The expiration date on labeling is incorrect. |
| Product | CM 50-001-01 Injectate Kit, accessory device to LiDCOunity v2 Monitor - Product Usage: intended to administer lithium dilution indicator (tube administrative set). |
| Quantity | 40 packs (5 each per pack) |
| Distribution | Worldwide distribution - US Nationwide distribution in the state of IL and the country of Kuwait. |
| Initiated | 2020-11-19 |
| Classified | 2020-12-30 |
| Terminated | 2022-09-26 |
| Recall number | Z-0756-2021 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Lidco Ltd (Z-0756-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/86825/
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