Perkinelmer Life Sciences, Inc. Angiotensin I [125I] Radioimmunoassay Kit, 250 Tube Catalog Number: NEA104 For in-vitro diagnostic use Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Angiotensin I [125I] Radioimmunoassay Kit, 250 Tube Catalog Number: NEA104 For in-vitro diagnostic use
Brand
Perkinelmer Life Sciences, Inc.
Lot Codes / Batch Numbers
Lot 181269, Expiration 8/27/03
Products Sold
Lot 181269, Expiration 8/27/03
Perkinelmer Life Sciences, Inc. is recalling Angiotensin I [125I] Radioimmunoassay Kit, 250 Tube Catalog Number: NEA104 For in-vitro diagnostic u due to Incorrect calibration standard value may result in 25% higher assay values for controls and patient samples. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Incorrect calibration standard value may result in 25% higher assay values for controls and patient samples
Recommended Action
Per FDA guidance
PerkinElmer notified all customers who received the lots by telephone by July 23, 2003 followed by letter dated July 25, 2003, which includes instructions for documenting receipt and lot removal either by destroying or returning product to PerkinElmer
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