FDA recall record

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 IIclassification
Z-0756-2021official record ID
Jan 6, 2021report date

Recall record at a glance

Official recordZ-0756-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmLidco Ltd
Report dateJan 6, 2021
Recall initiation dateNov 19, 2020
Quantity40 packs (5 each per pack)
LocationLondon, N/A, United Kingdom

Official product description

CM 50-001-01 Injectate Kit, accessory device to LiDCOunity v2 Monitor - Product Usage: intended to administer lithium dilution indicator (tube administrative set).

Why the product was recalled

The expiration date on labeling is incorrect.

Distribution information

Worldwide distribution - US Nationwide distribution in the state of IL and the country of Kuwait.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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