CLASS II Food recall · Reported 22 Jan 2014 · FDA Enforcement Report
Lobster Bisque recalled by Colony Brands
Colony Brands is recalling Lobster Bisque, product 45036, distributed in 13 states. The recall was initiated on 5 Dec 2013 and the FDA has classified it as Class II.
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-1386-2014
- FDA event ID
- 67051
- Recalling firm
- Colony Brands, Monroe, WI
- Brand
- Lobster Bisque
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 5 Dec 2013
- FDA classified
- 10 Jan 2014
- Reported
- 22 Jan 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Undeclared Wheat & Gluten
- Product category
- Soup
Timeline
| 5 Dec 2013 | Recall initiated by company | |
| 10 Jan 2014 | Classified by FDA | +36 days |
| 22 Jan 2014 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Lobster Bisque contains undeclared wheat allergen.
Product as listed by the FDA
Lobster Bisque, product 45036. Net WT 4.0 lbs. Keep Frozen.
Where it was distributed
OK, TX, NY, ND, FL, PA, CA, CO, NV, AL, MI, AR, MA.
AlabamaArkansasCaliforniaColoradoFloridaMassachusettsMichiganNorth DakotaNevadaNew YorkOklahomaPennsylvaniaTexas
Questions about this recall
Why was it recalled?
Lobster Bisque contains undeclared wheat allergen.
Which lots are affected?
Lot number 3418130
Where was it sold?
OK, TX, NY, ND, FL, PA, CA, CO, NV, AL, MI, AR, MA.
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 II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
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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