CM 50-001-01 Injectate Kit — Class II medical device recall Z-0756-2021
Terminated recall by Lidco Ltd, reported 2021-01-06, distributed nationwide. The expiration date on labeling is incorrect.
| Recall number | Z-0756-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Lidco Ltd, London, N/A, United Kingdom |
| Recall initiated | 2020-11-19 |
| Classified | 2020-12-30 |
| Reported by FDA | 2021-01-06 |
| Terminated | 2022-09-26 |
| Distributed | Nationwide (US) |
| Countries outside the US | KW |
| Reason classes | labeling |
| Lot numbers | 11090135, 11103786 |
| Model numbers | 50-001-01 |
| Expiration dates | 2023-02, 2023-04-26 |
Product
CM 50-001-01 Injectate Kit, accessory device to LiDCOunity v2 Monitor - Product Usage: intended to administer lithium dilution indicator (tube administrative set).
Reason for recall
The expiration date on labeling is incorrect.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0756-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.