CLASS I Food recall · Reported 10 Nov 2021 · FDA Enforcement Report
Cedar s Organic Mediterranean Hommus recalled
Cedar's Mediterranean Foods is recalling Cedar s Organic Mediterranean Hommus, distributed in 23 states. The recall was initiated on 25 Oct 2021 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-0134-2022
- FDA event ID
- 88925
- Recalling firm
- Cedar's Mediterranean Foods, Ward Hill, MA
- Brand
- Cedar
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 25 Oct 2021
- FDA classified
- 9 Nov 2021
- Reported
- 10 Nov 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Tree Nuts
- Product category
- Other
Timeline
| 25 Oct 2021 | Recall initiated by company | |
| 9 Nov 2021 | Classified by FDA | +15 days |
| 10 Nov 2021 | Published in enforcement report | +1 day |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
May contain undeclared tree nuts (pine nuts)
Product as listed by the FDA
Cedar s Organic Mediterranean Hommus 10 oz.
Where it was distributed
MA, FL, GA, NC, OR, OK, LA, AZ, CO, WI, MD, OH, CA, NV, NM, UT, MO, ME, NY, KS, AL, TN, MN,
AlabamaArizonaCaliforniaColoradoFloridaGeorgiaKansasLouisianaMassachusettsMarylandMaineMinnesotaMissouriNorth CarolinaNew MexicoNevadaNew YorkOhioOklahomaOregon
Questions about this recall
Why was it recalled?
May contain undeclared tree nuts (pine nuts)
Which lots are affected?
UPC Code: 044115403028 Sell by Date DEC 12, 2021 (32I21).
Where was it sold?
MA, FL, GA, NC, OR, OK, LA, AZ, CO, WI, MD, OH, CA, NV, NM, UT, MO, ME, NY, KS, AL, TN, MN,
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 26 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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