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FDA Medical Device Recalls (openFDA)

Nichols Institute Diagnostics: Nichols Advantage EPO Calibration Verifiers, Catalog #63-7512

Recall number
Z-0136-06
Recalling firm
Nichols Institute Diagnostics
Product
Nichols Advantage EPO Calibration Verifiers, Catalog #63-7512
Status
Terminated
Initiated
2005-09-30
Posted
2005-11-15
Terminated
2012-03-16
Reason
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.
Root cause
Other
Action
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.
Quantity
215
Distribution
CA, IN, WA
Lot, serial or model codes
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.
510(k) numbers
not on file
PMA numbers
not on file
Product code
GGT
Firm FEI
2050095
Firm city
San Clemente
Firm state
CA
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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