CLASS I Food recall · Reported 2 May 2018 · FDA Enforcement Report

Bloody Hell Mary, HOT, Kitchen By The Sea, From the Beach House recalled

Kitchen By The Sea is recalling Bloody Hell Mary, HOT, Kitchen By The Sea, From the Beach House. The recall was initiated on 20 Mar 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBM Batch # 41B19217A,41B21517A,41B26117A,41B29817A,41B32617A,41B34817A
Quantity recalled11 quarts (352 ounces)

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-1137-2018
FDA event ID
79675
Recalling firm
Kitchen By The Sea, Panama City Beach, FL
Classification
Class I
Status
Terminated
Recall initiated
20 Mar 2018
FDA classified
26 Apr 2018
Reported
2 May 2018
Type
Voluntary: Firm initiated
Customers notified by
Visit
Reason category
Undeclared Sulfites
Product category
Other

Timeline

20 Mar 2018Recall initiated by company
26 Apr 2018Classified by FDA+37 days
2 May 2018Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

allergen warning not listed on labels , egg, soy and wheat including sulfites

Product as listed by the FDA

Bloody Hell Mary, HOT, Kitchen By The Sea, From the Beach House, Net Wt. 32 oz. (.9L), Low Sodium

Where it was distributed

U.S. consignees only.

Questions about this recall

Why was it recalled?

allergen warning not listed on labels , egg, soy and wheat including sulfites

Which lots are affected?

BM Batch # 41B19217A,41B21517A,41B26117A,41B29817A,41B32617A,41B34817A

Where was it sold?

U.S. consignees only.

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.

Other products in this recall event

1 other product · FDA event 79675

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