Recall StatusOpen, Classified
Date Initiated2024-08-29
Product Quantity1649
Reason for Recall
Contaminated equipment and packaging caused Klebsiella oxytoca, Enterobacter asburiae, Enterobacter bugandensis, pathogenic and opportunistic bacteria, to occur in ultrasonic detergent, which caused product bloating/leaking, and if used during medical/dental procedures could result in urinary tract, respiratory, bloodstream infections; workers handling contaminated product/instruments also at risk
Firm Action
On 8/29/24, recall notices were mailed to customers who were asked to do the following:
1) This recall notice should be shared with anyone who needs to be aware within your
organization and forwarded to any organization where potentially affected devices have
been transferred. This recall should be carried out to the user level.
2) If your company repacked these medical devices into convenience kits or into other
packaging, please contact your local FDA recall coordinator to evaluate the need for
a new recall (https://www.fda.gov/safety/industry-guidance-recalls/ora-recallcoordinators).
3) Return partially-used or unused product to the recalling firm.
4) Complete and return the response form via email to
[email protected]
If you have any questions, contact the firm at 303-529-5937 or the email above.
Root Cause
Material/Component Contamination
Distribution Pattern
Worldwide - US Nationwide distribution in the states of MN, GA, PA, WA, CO, NY, MD, CA, MI, NE, UT, OK, WI, NJ, IL, ME, CT, KS, TX, NC, TN, SC, MO and the countries of Canada.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.