Diasorin Inc. 1,25-Dihydroxyvitamin D RIA Kit -For the quantitative determination of 1,25 Dihydroxyvitamin D in serum or EDTA plasma-DiaSorin, Stillwater, Minnesota 55082-0285, USA Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
1,25-Dihydroxyvitamin D RIA Kit -For the quantitative determination of 1,25 Dihydroxyvitamin D in serum or EDTA plasma-DiaSorin, Stillwater, Minnesota 55082-0285, USA
Brand
Diasorin Inc.
Lot Codes / Batch Numbers
Catalog #65100E. Kit Lot #''s 117139, 117140, 1117141
Products Sold
Catalog #65100E. Kit Lot #''s 117139, 117140, 1117141
Diasorin Inc. is recalling 1,25-Dihydroxyvitamin D RIA Kit -For the quantitative determination of 1,25 Dihydroxyvitamin D in se due to Potential for the DiaSorin Kit 1,25-Dihydroxyvitamin D RIA Kit Control 1 (lot 548520) & 2 (lot 548521) to recover out of the defined range, LOW. (I. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential for the DiaSorin Kit 1,25-Dihydroxyvitamin D RIA Kit Control 1 (lot 548520) & 2 (lot 548521) to recover out of the defined range, LOW. (If one or both of the kit controls recover outside the defined range, the run is considered invalid)
Recommended Action
Per FDA guidance
Product recalled by letter dated 6/01/2006
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 noticeDistribution
As reported by FDA
CA, CO, CT, GA, IL, IN, KS, MI, MN, NV, NY, NC, UT, VT, VA
Page updated: Jan 10, 2026