FDA's Small-Restaurant Traceability Draft: What It Would Change and What to Check Now

FDA's October 2026 guidance is a draft. Even if finalized, it would be nonbinding enforcement discretion for some smaller restaurants and retailers, not an exemption. What it would cover, why its dollar figures aren't current cutoffs, and a worksheet.

Ryan Speier

No. FDA's October 2026 proposal is a draft, not a new exemption, and it doesn't tell anyone to stop keeping records. FDA marks the guidance "Draft" and "Not for implementation." If FDA finalizes it as written, FDA says it would not enforce any of the Food Traceability Rule's requirements for restaurants and retail food establishments whose average annual value of food sold or provided over the previous three years is more than $250,000 and no more than $1 million. Those two numbers are 2020 base figures that FDA adjusts for inflation, and FDA hasn't posted the adjusted traceability figures yet.

So don't drop your preparation, and don't rush into buying a traceability system either. Use the time to pull together your sales history, the foods you buy that are on FDA's Food Traceability List, and the questions you still need answered. The worksheet below helps with that. It won't tell you whether you're covered, and this isn't legal advice.

What we read, on October 14, 2026: FDA's October 8 constituent update, the draft guidance page and its five-page PDF, FDA's current traceability rule overview, the Food Traceability List and FDA's inflation-adjusted cut-offs page. The official eCFR site returned an access-check page instead of the current regulation text (21 CFR Part 1, Subpart S), so the rule details here are as FDA describes them on those pages.

What food traceability is, and what it isn't

The Food Traceability Rule is FDA's extra recordkeeping rule for specific higher-risk foods. Covered businesses keep records of key events in a listed food's trip through the supply chain, such as receiving and shipping, so FDA can trace a contaminated food back quickly during an outbreak. FDA's draft sums up what a covered business has to do: keep the required records for 2 years, get them to FDA within 24 hours of a request (or a reasonable time FDA agrees to), send an electronic sortable spreadsheet when FDA needs one for an outbreak, recall or other public health threat, and keep a written traceability plan.

It only reaches foods on the Food Traceability List, plus foods that contain a listed food as an ingredient while that ingredient stays in the same form, such as fresh. The list includes fresh leafy greens, fresh tomatoes, peppers, cucumbers and herbs, fresh melons, shell eggs, many soft cheeses, nut butters, and a long run of finfish and shellfish. Each entry has its own inclusions and exclusions, so read the list itself rather than going by the category name.

Receiving is one of the events FDA lists. Selling food to a guest isn't "shipping" in FDA's description, but sending food from one of your addresses to another, like a commissary supplying your restaurants, does count as shipping and receiving.

Two things this rule is not:

  • It isn't FDA food facility registration. Whether a location has to register with FDA is a separate rule with its own exemptions. Our FDA facility registration renewal answer covers that, and its consumer-sales test has nothing to do with the traceability dollar figures.
  • It isn't a recall notice. When a recall hits, you act on that notice using your invoices and receiving records, whether or not this rule applies to you. Our Star Meat recall answer walks through that process.

Three kinds of relief, plus a separate timing question

These get blurred together easily. The table's first row explains how to read the dollar figures, and it applies to every row after it.

What it isWho FDA describesWhat it doesStatus
How to read every dollar figure in this table2020 base figures that FDA adjusts for inflation. FDA hasn't posted the adjusted traceability figures, so there's no current cutoff to compare againstEach figure applies to the average annual value of food sold or provided over the previous three years, on a rolling basis. One year's sales isn't that averageNot an eligibility test. Don't decide which row you're in from these base figures
Full small retail and restaurant exemptionRestaurants and retail food establishments whose rolling three-year average of annual food sold or provided is no more than the $250,000 base figure, as adjusted for inflationFully exempt from the ruleAlready an exemption in the rule, as FDA describes it on page 4 of the draft (21 CFR 1.1305(i)). Adjusted figure not posted
Spreadsheet-format reliefRestaurants and retail food establishments otherwise covered, whose rolling three-year average is more than the $250,000 base figure and no more than the $1,000,000 base figure, both as adjusted for inflationNo electronic sortable spreadsheet requirement; they can give FDA the required information in another format. The other requirements still applyAlready part of the rule, as FDA describes it on page 4 of the draft (21 CFR 1.1455(c)(3)(iii)(B)). Adjusted figures not posted
Proposed enforcement discretionThe same middle band: rolling three-year average more than the $250,000 base figure and no more than the $1,000,000 base figure, both as adjusted for inflationFDA would not intend to enforce any of the rule's requirements. It's nonbinding and the rule stays in place. Even if finalized, it's enforcement discretion, not an exemptionDraft only, not for implementation. Has no effect unless finalized. FDA asks for comments by November 23, 2026
General enforcement timingEveryone subject to the ruleFDA says it intends to follow Congress's directive not to enforce the rule before July 20, 2028Separate from the draft. FDA still describes the change of compliance date to July 20, 2028 as proposed, not final

"Enforcement discretion" means FDA saying it doesn't intend to enforce a requirement that still exists. FDA's draft says that, when finalized, it will represent FDA's current thinking, that it doesn't establish any rights for anyone and that it isn't binding on FDA or the public. FDA also says it expects to keep the policy going while it studies these operators' challenges and possible solutions. That's a stated intention, not a permanent carve-out, and right now it isn't even final.

Why FDA did this: the draft says many of these operators are over the $250,000 base figure but still small enough that they struggle to stay in business, run with very small staffs and lack the resources for the training, technology and staffing the rule would take. It says spreadsheet relief helps many of them, but they still struggle to meet all of the rule's other requirements.

The timing piece, and a stale date to ignore

The rule's original compliance date was January 20, 2026. According to footnote 3 of the October draft and the Compliance Date section of FDA's rule overview, FDA proposed in August 2025 to move it to July 20, 2028 (90 FR 38084). Congress then directed FDA, in the Continuing Appropriations, Agriculture, Legislative Branch, Military Construction and Veterans Affairs, and Extensions Act of 2026, not to enforce the rule before July 20, 2028, and FDA says it intends to comply. The pages we read still call the date change a proposal, so don't treat it as a finalized amendment. FDA adds that it expects the draft small-business policy to be in effect, if finalized, by the time the compliance date arrives.

One trap: further down that same overview page, which FDA updated October 8, a "Getting Started" section still says the compliance date is January 20, 2026. That's the original date. The page's own Compliance Date section and the October draft explain what changed.

The inflation adjustment isn't posted yet

FDA's FSMA inflation-adjusted cut-offs page (content current as of May 13, 2026) says FDA intends to post the traceability values "in future updates." The tables above that section are for other FSMA rules, with their own dollar thresholds, and they can't stand in for the traceability figures.

Until FDA posts them:

  • Don't treat $250,000 or $1 million as today's cutoffs. They're base figures.
  • Don't borrow a cutoff from a different FSMA rule.
  • Don't make up your own inflation factor. The adjusted figures will differ from the base figures, and that matters most when your average lands close to either line.

How to work out a three-year average

This example uses a made-up business, Juniper Street Café, with one location. The numbers are invented for teaching. It uses calendar years only to show the arithmetic; which twelve-month periods FDA counts is one of the questions to confirm.

PeriodFood sold or provided (dollars as recorded that year)
2023$812,400
2024$868,900
2025$931,700
Three-year total$2,613,000
Average (total ÷ 3)$871,000 a year

The example stops there. The $871,000 is an average of each year's recorded dollars. Whether it falls in any band depends on FDA's adjusted figures, which periods count, and what counts as food sold or provided. None of that is settled in the sources we read. And the middle-band policy is still a draft, so even a confirmed average wouldn't put an exemption in place.

Three mistakes that change the answer:

  • Using one year. 2025 alone is $931,700. The three-year average is $871,000.
  • Treating a missing year as zero. If 2023's records couldn't be found and someone wrote $0, the "average" would come out at $600,200, which is $270,800 too low. A missing year is unknown, not zero.
  • Averaging only the years you have. Dividing 2024 and 2025 by two gives $900,300. That isn't a three-year average either. Mark the gap as unknown and go find the records.

If you've been open less than three years, or had a partial year, FDA's draft doesn't say how that's handled. Don't guess. Put it on your question list.

Questions to confirm before deciding anything

QuestionWhy it mattersWhere it stands (October 14, 2026)
What counts as "food sold or provided"? Think alcohol and other beverages, non-food merchandise, sales tax, tips and service charges, catering and delivery-app ordersChanges the total you averageNot defined in the FDA pages we read
How is food you didn't sell valued: comps, donations, staff meals?The draft says "sold or provided," but doesn't explain the valuationNot explained
Which three years, and how does "rolling" work: calendar or fiscal year?Sets which records you pullNot explained
Are several locations or related companies counted together or separately?Could move you across a lineNot addressed
Less than three years open, or a closed or partial year?You may not have three full yearsNot addressed
What are the inflation-adjusted traceability figures?The actual lines you'd compare againstNot posted; FDA says it will post them
Is the guidance final, and did anything change?The draft has no effect until finalizedDraft, comments open until November 23, 2026
Do you receive any Food Traceability List foods?The rule only reaches listed foodsCheck the current list against your order guide

The draft names FDA's FSMA Technical Assistance Network as the place to send questions about it. FDA gives you a case number when you submit. FDA also has an online traceability exemptions flow chart for the rule's existing exemptions; we didn't run it for this answer and can't confirm it reflects the October draft. For any decision with legal weight, use your own attorney or food safety consultant.

Copyable worksheet

Fill this in with your own records and keep it private. Section 6 is only for an exemption that's already part of the rule and that you've confirmed. The October draft isn't an exemption, so it doesn't go there.

FOOD TRACEABILITY PREP WORKSHEET
Planning notes only. Not a coverage or exemption decision.

Prepared by: ____________   Date: ____________
Business / location(s): ______________________________

1. DRAFT STATUS
FDA small retail/restaurant enforcement policy (October 2026):
[ ] Still a draft, not for implementation
[ ] Finalized on: ________  Changes from draft: ________
Checked on FDA's guidance page, date: ________

2. WHAT WE DO
[ ] Restaurant  [ ] Retail food store  [ ] Other: ________
Other locations or related businesses: ________________
How FDA counts them: [ ] Confirmed (source: ______)  [ ] Unknown

3. FOOD TRACEABILITY LIST FOODS WE RECEIVE
List checked on (date): ________
Food | Supplier | Source/lot info we get today
____ | ________ | ____________________________
____ | ________ | ____________________________

4. FOOD SOLD OR PROVIDED, PREVIOUS THREE YEARS
What we counted / left out: ___________________________
Which periods count (calendar/fiscal, rolling):
[ ] Confirmed (source: ______)  [ ] Unknown
How food provided but not sold is valued:
[ ] Confirmed (source: ______)  [ ] Unknown
Period (start-end) | Amount ($) | Record used | Complete? (Y/N/Missing)
__________________ | __________ | ___________ | ________
__________________ | __________ | ___________ | ________
__________________ | __________ | ___________ | ________
Any year missing or partial: write UNKNOWN, never 0.
Three-year average, only if all three are complete: $________

5. FDA INFLATION-ADJUSTED TRACEABILITY FIGURES
[ ] Not posted as of (date): ________
[ ] Posted: $________ and $________  Year: ____
    Source URL: ______________________

6. EXISTING EXEMPTION WE RELY ON (not the October draft)
[ ] None established
[ ] Basis: ________  Confirmed by: ________  Source: ________

7. OPEN QUESTIONS
Question | Who owns it | Asked where (TAN case #) | Answer + date
________ | ___________ | ________________________ | _____________

What to do now

These are planning suggestions, not legal requirements.

  1. Keep the supplier invoices and receiving records you already keep. They help in any recall, and you'll want them if the rule ends up applying to you.
  2. Pull three years of sales records and note where each number came from. Mark any gap as unknown.
  3. Walk your order guide against the Food Traceability List. For each listed food, note the supplier and what source or lot information arrives on the invoice or case today. Our purchasing and receiving guide covers the receiving routine itself.
  4. Hold off on buying software just for this rule until you know whether it applies to you and FDA has finalized its policy. If you're choosing purchasing or inventory software anyway, ask what supplier and receiving records it can export, but treat that as its own decision.
  5. Send your open questions to FDA's Technical Assistance Network and keep the case number with your worksheet.
  6. Watch for the final guidance and the adjusted figures. If you want to weigh in, FDA takes comments on the draft through November 23, 2026 (docket FDA-2025-D-6952), and holds a free virtual public meeting on November 6, 2026. Registration is required, and speakers must register by October 26. Neither date is a compliance deadline.

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