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
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Recalling FirmMedline Industries Inc
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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