Recall StatusTerminated
Date Initiated2015-04-09
Date Terminated2017-03-22
Product Quantity155 kits
Reason for Recall
IMMULITE/IMMULITE 1000 TBG catalog LKTB lot 257 is failing the adjustment slope instrument parameter of <1.80. The resulting slope of the kit is >1.80 resulting in the potential to produce depressed TBG patient values.
Firm Action
Siemens sent an Urgent Field Safety Notice dated April 2015, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer.
Actions to be Taken by the Customer
Discontinue use and discard kit lot listed in Table 1.
Review your inventory of these products to determine your laboratory's replacement needs.
Please review this letter with your Medical Director.
Complete and return the Field Correction Effectiveness Check Form attached to this letter within thirty (30) days.
Please retain this letter with your laboratory records, and forward this letter to those who may have received this product.
We apologize for the inconvenience this situation may cause. If you have any questions, please contact your Siemens Customer Care Center or your local Siemens technical support representative. For further questions call (914) 631-8000.
Root Cause
Unknown/Undetermined by firm
Distribution Pattern
Worldwide Distribution to the countries of : Denmark, Spain, Great Britain, Germany, Bosnia Herzeg, China and Russian Federation.
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.