Nichols Institute Diagnostics Nichols Advantage EPO Calibration Verifiers, Catalog #63-7512 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Nichols Advantage EPO Calibration Verifiers, Catalog #63-7512
Brand
Nichols Institute Diagnostics
Lot Codes / Batch Numbers
Kit lots# 63-502081, 63-502081A contain Calibration Verifiers 1, 2, and 3. Lot #30-500952 is specific to Calibration Verifier 2, Lot #30-500953 is specific to Calibration Verifier 3.
Products Sold
Kit lots# 63-502081, 63-502081A contain Calibration Verifiers 1, 2, and 3. Lot #30-500952 is specific to Calibration Verifier 2; Lot #30-500953 is specific to Calibration Verifier 3.
Nichols Institute Diagnostics is recalling Nichols Advantage EPO Calibration Verifiers, Catalog #63-7512 due to Some units in Lot 30-500953 (Calibration Verifier 2) are mislabeled as Calibration Verifier 3. Some units of Lot 30-500953 (Calibration Verifier 3) ar. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Some units in Lot 30-500953 (Calibration Verifier 2) are mislabeled as Calibration Verifier 3. Some units of Lot 30-500953 (Calibration Verifier 3) are mislabeled as Calibration Verifier 2.
Recommended Action
Per FDA guidance
Written notification was sent via fax on 9/29/05. If receipt was not confirmed, written version of notification was mailed via next day delivery. NID intends to track the response forms and if after 2 weeks after distribution not all forms have been received, NID will conduct a follow-up phone call and resend if necessary.
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, IN, WA
Page updated: Jan 10, 2026