![]() Tote Box Meter, strips, alcohol swabs controls, lancets, ref guide Accu-Chek Inform II (wireless available - Blue light in Base unit) ![]() No data is lost if meter taken from docking station during download phase to patient test. Code Key is not mentioned here as the training is geared to nursing end users and they will never see it, only POCCs use the code key reader to input the lot numbers of reagents. ![]() ![]() But the meter can be used at any level of battery life, as it is charging tests per full charge. From a fully dead battery, if placed back in the base unit, it takes about 20 minutes to charge it enough to run a test. 6 hours to fully charge meter– Ideally, meters should always stay in base units. Docking the ACI II on the base unit when not in use will ensure that the meter is operational when required. Red is when you first plug in Base Unit to power outlet until meter gets put in it Explain the 3 components of the system emphasizing the charging function of the base unit. Inform II Quizīase Unit for automatic data transfer AND charging battery Green light when charging and sitting properly in Base unit. Perform a quality control test (QC) – Hands On 5. All other trademarks are the property of their respective owners.ġ. This record will be updated as the status changes.ACCU-CHEK, ACCU-CHEK INFORM, ACCU-CHEK PERFORMA and COBAS are trademarks of Roche. Learn more about medical device recalls.Ģ Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.ģ The manufacturer has initiated the recall and not all products have been corrected or removed. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Worldwide distribution - US Nationwide distribution.ġ A record in this database is created when a firm initiates a correction or removal action. Urgent Medical Device Correction(UMDC) by phone at 1-80 or on our website at under Contact Us for email or chat. Dispose of the affected test strips and vial according to your local guidelines.Ĭontact Accu-Chek Customer Care if you have questions regarding the information in this Complete and return the business reply letter to the recalling firm.ĥ. On our website at under Contact Us for email or chat. Contact Accu-Chek Customer Care for product replacement if you open a sealed carton and any of the vials inside meet the criteria listed above by phone at 1-80 or DO NOT perform control testing if you open a sealed carton and ay of the vials inside meet the criteria listed above.ģ. Anything prevents the cap from closing properlyĢ. You see any damage to the cap or vial, or The vial is open or damaged before using the test strips for the first time Check vials of affected test strips before use. Inappropriate therapy decisions based on inaccurate results could lead to adverse health consequences.ġ. Customers were warned that open vials may expose the test strips to humidity, which might damage the strips and result in inaccurate results (such as positively biased or falsely too high results). ![]() On July 28, 2021, the firm issued an Urgent Medical Device Correction to affected customers regarding the potential for open vials. An open vial might expose the test strips to humidity, which might damage the strips and result in inaccurate results, potentially leading to inappropriate therapy decisions and adverse health consequences. Test strip vials may open while inside sealed cartons during shipment. Since this is a labeling correction, this recall is not lot specific and is System, test, blood glucose, over the counter - Product Code NBWĪccu-Chek Inform II Test Strip, Whole Blood Glucose Test System, Model number 05942891001 Class 2 Device Recall AccuChek Inform II Test Strip ![]()
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