CLASS I Food recall · Reported 20 Oct 2021 · FDA Enforcement Report
Vemondo Vegan Crabless Mini Crabcakes by Lidl coated recalled
Cuisine Innovations Unlimited is recalling Vemondo Vegan Crabless Mini Crabcakes by Lidl coated, distributed in Maryland, North Carolina, Virginia. The recall was initiated on 24 Sep 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-0015-2022
- FDA event ID
- 88781
- Recalling firm
- Cuisine Innovations Unlimited, Lakewood, NJ
- Brand
- Vemondo
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 24 Sep 2021
- FDA classified
- 13 Oct 2021
- Reported
- 20 Oct 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Egg
- Product category
- Other
Timeline
| 24 Sep 2021 | Recall initiated by company | |
| 13 Oct 2021 | Classified by FDA | +19 days |
| 20 Oct 2021 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Undeclared egg
Product as listed by the FDA
Vemondo Vegan Crabless Mini Crabcakes by Lidl 8.5 OUNCES (240g) coated paper box ten (10) packages per case. Frozen.
Where it was distributed
Distributed to 3 distributors in MD, NC, and VA then further distributed to retail stores
MarylandNorth CarolinaVirginia
Stores named: Lidl
Questions about this recall
Why was it recalled?
Undeclared egg
Which lots are affected?
Lot # 23021: 2/17/2023 Lot # 23121: 2/18/2023 Lot # 23821: 2/25/2023
Where was it sold?
Distributed to 3 distributors in MD, NC, and VA then further distributed to retail stores
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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