Lower riskMedical device recall · FDA · Published November 19, 2020
Lidco CM 50-001-01 Injectate Kit: Incorrect Expiration Date on Label
Lidco recalls CM 50-001-01 Injectate Kit due to incorrect expiration date on labeling. This accessory for LiDCOunity v2 Monitor may expire before use, potentially causing safety issues.
“Lidco CM 50-001-01 Injectate Kit: Incorrect Expiration Date on Label.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/63846-lidco-cm-50-001-01-injectate-kit-incorrect-expiration-date. Based on FDA recall #Z-0756-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0756-2021%22&limit=1).
Lidco Ltd recalled the CM 50-001-01 Injectate Kit on Nov. 19, 2020, because its labeling bears an incorrect expiration date, according to the FDA. Owners should contact Lidco for a replacement.
How to tell if you have it
Brand: Lidco
Product: CM 50-001-01 Injectate Kit
Model: CM 50-001-01
Lot codes: 11103786, 11090135
Quantity: 40 packs
The hazard
The expiration date on the product labeling is incorrect, according to the FDA.
Context
GovInfoNow's records show other recent recalls of similar products include Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation (2026-05-13), B Braun Discofix Four Way Stopcock Recall (2026-08-04), and Medtronic Pocket Adaptor Kits with Incorrect Use-By Dates Recalled (2026-05-13).
How to tell if you have this one
Check the label for lot numbers 11103786 (expiration: 04/26/2023) or 11090135 (expiration: 02/2023). The kit is an accessory for LiDCOunity v2 Monitor used to administer lithium dilution indicator.
Brand
Lidco
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Expiration Date
Verify the expiration date on the label matches the correct date for your lot number.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Worldwide distribution - US Nationwide distribution in the state of IL and the country of Kuwait.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 22 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0756-2021 (November 19, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0756-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.