I failed a compliance test. How do I remediate and resubmit for retesting under OCM rules?
Remediation & Retest Workflow
Quarantine & notify the Office
Immediately place the entire lot on hold.
Email compliance@ocm.ny.gov with subject “Failed Lot Remediation – [License #]”.
Attach the failed Certificate of Analysis (COA) and outline the root-cause investigation you intend to run.
If you do not have this yet, we recommend sending the email without COAs initially to start the process and expedite the overall process.
Provide details of the intended remediation process you will use and information about your vendor if not performing in-house remediation.
Wait for acknowledgement before touching the lot (plan on ~2–3 business days).
Receive OCM instructions
OCM will confirm whether remediation is allowed or if destruction is mandatory (e.g., any prohibited-pesticide failure must be destroyed—no remediation permitted).
They may require a specific remediation approach (e.g., further extraction, dilution, or heat treatment).
Execute remediation
Follow the approved method exactly.
Update your batch record to document:
Lot/batch ID, equipment, processing line, and all corrective actions taken.
Keep the product in a clearly marked, locked area until retest results are received.
Prepare the lot for retest
Outcome handling
Pass:
Lab issues an amended COA incorporating all passing data with a note “Remediated Lot”, Updated QR code and provides the new COA to distributors/retailers before release.
Fail again:
The lot must be destroyed and logged in your inventory tracking system; no second remediation attempt is permitted.
Record-keeping & traceability
Retain all correspondence, revised COAs, destruction logs, and batch records for the life of the license.
Ensure your seed-to-sale system reflects every status change (quarantine, remediation, retest, release, or destruction).
Key points to remember
Only one remediation attempt per lot is allowed.
Never ship or transfer a lot while it is on administrative hold.
Treat remediation as a GMP activity—use validated equipment, calibrated instruments, and qualified personnel.