FDA recall record

Roche Diabetes Care Accu-Chek Aviva Plus Retail Strips 50 ct - intended for Blood Glucose recall — FDA Z-0998-2020

Inability to dose the test strips, may result in a temporary inability to get a result that could lead to a delay in treatment and/or therapy decisions

Class IIclassification
Z-0998-2020official record ID
Feb 12, 2020report date

Recall record at a glance

Official recordZ-0998-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmRoche Diabetes Care, Inc.
Report dateFeb 12, 2020
Recall initiation dateDec 11, 2019
Quantity92,836 vials
LocationIndianapolis, IN, United States

Official product description

Accu-Chek Aviva Plus Retail Strips 50 ct - intended for Blood Glucose Monitoring System Catalog Number: 06908217001

Why the product was recalled

Inability to dose the test strips, may result in a temporary inability to get a result that could lead to a delay in treatment and/or therapy decisions

Distribution information

Nationwide: Foreign: Austalia, India

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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