Medical device recalls Moderate risk

Medline Industries product recalled over sterility concerns

Recall date
September 14, 2020
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Official notice title
Medline Industries Inc recalls Kit Model #650301023, MTO Radiology Kit Cleveland Clinic - Product Usage: NAMIC Cath Lab and Interventional Radiology (…
Recall number
Z-0063-2021
FDA classification
Class II
Brand / firm
Medline Industries Inc
Sold / distributed
US Nationwide distribution including in the states of CA, CO, CT, OH, TX, and NY.

Why it was recalled

Non-sterile kits intended to be sterilized prior to use were sold to accounts without sterilization capabilities.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Kit Model #650301023, MTO Radiology Kit Cleveland Clinic - Product Usage: NAMIC Cath Lab and Interventional Radiology (IR) Kits consist of any combination of devices from the NAMIC Fluid Management finished good product families and potentially other devices designed and manufactured by original equipment manufacturers (OEM).

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