CLASS I Food recall · Reported 12 Aug 2020 · FDA Enforcement Report
Chantilly Key Lime Tartlets recalled by Whole Foods Market
Whole Foods Market is recalling Chantilly Key Lime Tartlets, distributed in Connecticut, Massachusetts, Maine, New Hampshire, Rhode Island. The recall was initiated on 23 Jul 2020 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-1048-2020
- FDA event ID
- 86117
- Recalling firm
- Whole Foods Market, Austin, TX
- Brand
- Chantilly Key
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 23 Jul 2020
- FDA classified
- 4 Aug 2020
- Reported
- 12 Aug 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Other
- Reason category
- Undeclared Tree Nuts
- Product category
- Oysters & Shellfish
Timeline
| 23 Jul 2020 | Recall initiated by company | |
| 4 Aug 2020 | Classified by FDA | +12 days |
| 12 Aug 2020 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Potential to contain undeclared tree nuts (almond)
Product as listed by the FDA
Chantilly Key Lime Tartlets Net Wt 1 oz. individually packaged in plastic clamshell containers with Whole Foods Market scale labels, a PLU code of 268564
Where it was distributed
Connecticut, Maine, Massachusetts, New Hampshire and Rhode Island
ConnecticutMassachusettsMaineNew HampshireRhode Island
Stores named: Whole Foods
Questions about this recall
Why was it recalled?
Potential to contain undeclared tree nuts (almond)
Which lots are affected?
PLU code of 2685640000, and product sell-by date through July 26, 2020
Where was it sold?
Connecticut, Maine, Massachusetts, New Hampshire and Rhode Island
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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