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Immucell Corp.

Launch the Re-Tain product

Not delivered by the deadline

AI-confirmed · human review in progress Independent AI checks agreed on primary SEC or regulator evidence. Records are now being reviewed by hand, starting with those our customers order.

Announced
7 Jan 2021
Due
30 Sep 2021
Checked
25 Oct 2026
  • Deadline
  • Met
  • Late
  • Not met
  • Today

What the company said

“we are planning for product launch during the third quarter of 2021 in the event of a first-time approval from the FDA”
  • SourceImmucell Corp. Form 8-K press release, 2021-01-07
  • FilingSEC filing index
  • Deadline as statedduring the third quarter of 2021
  • Deadline used30 Sep 2021, the last day of the stated period
  • TypeProduct
  • Permanent referenceKI-C-2021-ICCC-021293
    Cite as https://keptindex.org/c/KI-C-2021-ICCC-021293/ — this address never changes.

What we found

Evidence strength A What the grades mean

The company did not launch Re-Tain by the third quarter of 2021, as it had not yet received the final FDA approval required for commercial sales.

  • A
    Immucell Corp. 10-Q filed 2021-11-15 Regulatory filing · published 15 Nov 2021 · retrieved 25 Oct 2026 · kept permanently by the SEC · fingerprint ab0dfa76d631
    “approval of the CMC Technical Section is the fifth and final significant step required before Re-Tain® product sales can be initiated in the United States.” ✓ confirmed on the page
  • A
    Immucell Corp. 10-Q filed 2022-05-12 Regulatory filing · published 12 May 2022 · retrieved 25 Oct 2026 · kept permanently by the SEC · fingerprint 4d5296370bd4
    “The commercial introduction of this product in the United States requires us to obtain FDA approval. We have disclosed a timeline of events that could lead to product approval during the fourth quarter of 2022.” ✓ confirmed on the page

Market reaction: the shares moved -1.9% against the S&P 500 over the three sessions around the disclosure (12 Nov 2021 to 17 Nov 2021). What this measures

Checked 25 Oct 2026.

Commitment DNA

The structured record of this commitment. Fields the company did not state are left blank rather than guessed.

Event type
Commercial launch
Indicative materiality
Medium rules
Action
Launch
Deliverable
Re-Tain product
In the company’s control
Medium
Specificity
High
Conditional
Yes: in the event of a first-time approval from the FDA
Depends on
Regulatory

How this entry was checked

  1. Commitment recordedThe company's words were matched word for word against the filing.
  2. First checkAn AI model, Gemini (Google), read the company's later filings and recorded the outcome with a quoted passage.
  3. Second check: agreesA different AI model, Claude (Anthropic), re-read the evidence without being told the outcome and reached the same answer.
  4. Third check on a negative finding: agreesBecause a negative finding could harm a company if wrong, a stronger model re-read the evidence fully blind and reached the same answer.

Confirmed. This outcome counts towards the company's Kept Score. How verification works

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