Recall StatusOpen, Classified
Date Initiated2024-04-30
Product Quantity431
Reason for Recall
A cart with prefiltration drawer, an optional hemodialysis system accessory, has a cord with a female connector that has internal contact pins that may become damaged that could create localized heat, sparks, smoke, melting or charring (thermal event) of the female connector or the associated connector power entry module, which may lead to transient delay in treatment or blistering to the user.
Firm Action
On 4/30/24, correction notices were sent to customers asking them to do the following:
The firm has enclosed the replacement power cord (PN-0008460) with this communication based on the number of affected devices at your facility.
Disseminate this information to appropriate personnel within your facility for processing and distribution. This notice should be shared with any organization where the potentially affected devices have been transferred.
Follow instructions to replace the power cords. Dispose of the affected power cords.
Complete and return the acknowledgement and receipt form via email to
[email protected]
If you have questions or notice any damage around the power cord, please contact us at
[email protected] or 844-MYTABLO (844-698-2256) and request an inspection from a Field Service Engineer.
Distribution Pattern
US Nationwide distribution in the states of FL, CA, NC, GA, MD, DE, AK, OK, MA, WV, IN, KY, AZ, LA, NE, KS, NJ, CT, NM, CO, SC, TX, PA, NY, OH.
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.