Diasorin Inc. LIAISON 25-OH Viatamin D Kit, Vitamin D test system, Model Number 310900, DiaSorin Inc, Stillwater, MN 55082 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
LIAISON 25-OH Viatamin D Kit, Vitamin D test system, Model Number 310900, DiaSorin Inc, Stillwater, MN 55082
Brand
Diasorin Inc.
Lot Codes / Batch Numbers
Lot Numbers: 120422 and 120423.
Products Sold
Lot Numbers: 120422 and 120423.
Diasorin Inc. is recalling LIAISON 25-OH Viatamin D Kit, Vitamin D test system, Model Number 310900, DiaSorin Inc, Stillwater, due to Inaccurate measurements: Kits may sporadically recover kit and external control values out of range high.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Inaccurate measurements: Kits may sporadically recover kit and external control values out of range high.
Recommended Action
Per FDA guidance
Consignees were notified by a Diasorn Customer Notification Letter sent by email on 2/1/08. The letter instructs users to stop using the affected kits, destroy any kits remaining in inventory and to return a response form in order to receive replacement product. For additional information contact 1-800-328-1482.
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 noticeDistribution
As reported by FDA
AR, CA, GA, IL, IA, MD, MA, MI, MN, MO, NJ, NM, NY, NC, OR, PA, TN, UT, WA
Page updated: Jan 10, 2026