Recall StatusOpen, Classified
Date Initiated2020-03-03
Product Quantity15
Reason for Recall
Bolts holding the longitudinal movement of catheterization tables may be loose, which may lead to table surface/top tilting.
Firm Action
On 03/03/20, Urgent Medical Device Correction notices were mailed to Radiology Managers/Directors. To correct this issue, the bolts holding the longitudinal movement of the table will need to be inspected to determine if the bolts are tightened to specification. Recalling firm service representatives will contact customers to set up appointments to inspect bolts. Radiology Managers/Directors were advised of the following:
a) Should this problem occur before your appointment with the recalling firm's service representative, please stop using the system and contact the service representative.
b) If abnormalities are found operating the table during a procedure, please stop use, and contact the service representative.
c) Share this information with all users and reviewing radiologists as well as clinical engineering, and the biomedical group at your facility.
d) Complete and return the Customer Reply Form.
Additional questions should be directed to (800) 421-1968 or your local service representative (800) 521-1968
Root Cause
Process control
Distribution Pattern
US Nationwide distribution including in the states of PA, AR, OH, NC, CA, IA, GA, IL, AL, WV, LA, MO, FL, MS, TX, AZ, MA, NJ, MD, NY, NV, OK, WI, PR.
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.