Medline Industries Inc EVENCARE G3 Blood Glucose Test Strips, 1 test strip per foil pouch, 50 foil pouches per box, 12 boxes per case. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
EVENCARE G3 Blood Glucose Test Strips, 1 test strip per foil pouch, 50 foil pouches per box, 12 boxes per case.
Brand
Medline Industries Inc
Lot Codes / Batch Numbers
Model Number: MPH3550FL, Lot number: 16819023001, Expiration Date: 11/12/2020
Products Sold
Model Number: MPH3550FL, Lot number: 16819023001, Expiration Date: 11/12/2020
Medline Industries Inc is recalling EVENCARE G3 Blood Glucose Test Strips, 1 test strip per foil pouch, 50 foil pouches per box, 12 boxe due to Incomplete seal and premature expiration of individually packaged Blood Glucose Test Strips.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Incomplete seal and premature expiration of individually packaged Blood Glucose Test Strips.
Recommended Action
Per FDA guidance
Medline Industries, Inc. notified customers on about 09/18/2019, via "URGENT RECALL IMMEDIATE ACTION REQUIRED" letter. Customers were informed that the heat activated adhesive used to seal the foil pouch was not fully cured during the manufacturing process. As a result, an incomplete seal and premature expiration of the individually packaged Blood Glucose Test Strips has occurred. Inspection using EVENCARE G3 control solution and unused Blood Glucose Test Strips, from the affected lot, has shown that the test strips can produce inaccurate blood glucose readings. Instructions included to immediately check inventory for the affected item and lot number, quarantine affected product, complete and return the enclosed response form, arrange for the return of all affected product, and notify customers if the product was further distributed. Questions can be directed to 866-359-1704.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026