ClearanceBrief
Recall Z-2351-2021 ยท LZG Pump, Infusion, Insulin

Roche Diabetes Care, Inc.

Accu-Chek Aviva Plus Test Strip, Blood Glucose Monitoring System, Model numbers: 06908152001, 06908217001, 06908268001, 06908349001, 06908373001

DateJul 28, 2021
StatusOpen, Classified
ReasonTest strip vials may open while inside sealed cartons during shipment. 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.
Root causePackage design/selection
ActionOn July 28, 2021, the firm issued an Urgent Medical Device Correction to affected customers regarding the potential for open vials. 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). Inappropriate therapy decisions based on inaccurate results could lead to adverse health consequences. ACTIONS REQUIRED BY USERS: 1. Check vials of affected test strips before use. DO NOT use test strips if: - The vial is open or damaged before using the test strips
Quantity10,546,420 (US), 19,120,668 (OUS)
DistributionWorldwide distribution - US Nationwide distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K131029ACCU-CHEK AVIVA PLUS TEST STRIP
Roche Diagnostics Operations, Inc., Aug 9, 2013