CLASS II Food recall · Reported 1 Jan 2014 · FDA Enforcement Report
Phillips Food Service Lobster Bisque cryobag, frozen recalled
Kettle Cuisine is recalling Phillips Food Service Lobster Bisque cryobag, frozen, distributed in Connecticut, Illinois, Massachusetts, Maryland, New York, Wisconsin. The recall was initiated on 26 Nov 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-1138-2014
- FDA event ID
- 66994
- Recalling firm
- Kettle Cuisine, Chelsea, MA
- Brand
- Phillips
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 26 Nov 2013
- FDA classified
- 23 Dec 2013
- Reported
- 1 Jan 2014
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Wheat & Gluten
- Product category
- Soup
Timeline
| 26 Nov 2013 | Recall initiated by company | |
| 23 Dec 2013 | Classified by FDA | +27 days |
| 1 Jan 2014 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product contains undeclared wheat
Product as listed by the FDA
Phillips Food Service Lobster Bisque, 4 lb cryobag, frozen Item #45036
Where it was distributed
MD, CT, IL, NY, MA WI
Questions about this recall
Why was it recalled?
Product contains undeclared wheat
Which lots are affected?
Code Dates: 3433830, 3401830, 3405330, 3406530, 3411530,3412030, 3412930, 3418130 Sell By dates from: 12/4/14 through 6/30/2015
Where was it sold?
MD, CT, IL, NY, MA WI
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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