Recall StatusOpen, Classified
Date Initiated2023-06-02
Product Quantity6902
Reason for Recall
Cell Collection Device may be at increased risk of the sponge detaching from the string during removal of the device from the patient, which could lead to device fragments in patient, obstruction, airway obstruction, secondary intervention, secondary intervention (with the primary procedure), supraglottic airway obstruction, and aspiration.
Firm Action
On 6/2/23, Medtronic sent recall notices to customers who were informed of the following:
1) If product was purchased directly from Medtronic, return affected product to Medtronic.
2) If product was purchased from a distributor, return affected product to the distributor.
3) The recall notice should be passed on to all who need to be aware within your organization or to any organization where the potentially affected product has been transferred.
4) Complete and return the Customer Confirmation Form to
[email protected]
Adverse reactions or quality problems experienced with this product can be reported to Technical Support at
[email protected] or call 1-800-448-3644 option 3.
Root Cause
Process control
Distribution Pattern
Worldwide - US Nationwide distribution in the states of NY, MN, VA, WI and the countries of Canada, Netherlands, Poland, United Kingdom.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.