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Terminated

Kit Model #65193091, MTO Left Heart Kit - 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).

FDA Recall Z-0068-2021 · Posted None

Recall StatusTerminated
Product CodeOEQ
Date Initiated2020-09-14
Date Terminated2021-04-09
Product Quantity16 kits

Reason for Recall

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

Firm Action

Medline Industries, Inc. had provided each consignee with a response form to return via email. Each Response received will be recorded and the firm will send subsequent letters to consignees that have not provided a response to our recall notification in the allotted time. Medline has provided each consignee with a response form to return or email. Each Response received will be recorded and the firm will send subsequent letters to consignees that have not provided a response to the field action notification in the allotted time.

Root Cause

Process design

Distribution Pattern

US Nationwide distribution including in the states of CA, CO, CT, OH, TX, and NY.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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