Diasorin Inc. 25-Hydroxyvitamin D 125 I RIA Kit, in vitro diagnostic. REF:68100E DiaSorin Stillwater, Minnesota 55082-0285, U.S.A. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
25-Hydroxyvitamin D 125 I RIA Kit, in vitro diagnostic. REF:68100E DiaSorin Stillwater, Minnesota 55082-0285, U.S.A.
Brand
Diasorin Inc.
Lot Codes / Batch Numbers
Part # 68100E, lot # 119604A
Products Sold
Part # 68100E, lot # 119604A
Diasorin Inc. is recalling 25-Hydroxyvitamin D 125 I RIA Kit, in vitro diagnostic. REF:68100E DiaSorin Stillwater, Minnesota 5 due to 25 Hydroxyvitamin D RIA kits may contain the incorrect lot of tracer.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
25 Hydroxyvitamin D RIA kits may contain the incorrect lot of tracer.
Recommended Action
Per FDA guidance
Consignees were notified by phone on 8/21/07 followed by a written notification by Fax or email. The letter described the product and problem and recommended to inspect the kits and to destroy all tracer vials of lot number 726023. They also requested the consignee to return the findings by fax or mail.
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