Becton Dickinson & Company BD Latitude (DMS) -- Blood Glucose Monitor. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
BD Latitude (DMS) -- Blood Glucose Monitor.
Brand
Becton Dickinson & Company
Lot Codes / Batch Numbers
All lots under the following Catalog numbers: 322050, 322000, 322015, 322067.
Products Sold
All lots under the following Catalog numbers: 322050; 322000; 322015; 322067.
Becton Dickinson & Company is recalling BD Latitude (DMS) -- Blood Glucose Monitor. due to BD Blood Glucose Monitors may inadvertently switch the Unit of Measure from mg/dL to mmol/L or vice versa during battery insertion or when a meter is . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
BD Blood Glucose Monitors may inadvertently switch the Unit of Measure from mg/dL to mmol/L or vice versa during battery insertion or when a meter is dropped.
Recommended Action
Per FDA guidance
Recall notifications letters began mailing on 1/5/2006 to distributors, retailers, and DME providers. Healthcare professionals and consumers mailings will be during the week of 1/9/2006
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