CLASS II Food recall · Reported 22 Jan 2020 · FDA Enforcement Report

Seafood Lobster Dip recalled by Wegmans Food Markets

Wegmans Food Markets is recalling Seafood Lobster Dip, distributed in 7 states. The recall was initiated on 9 Jan 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll Codes UPC: 2-06332-00000
Quantity recalledVaries by store.

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-0545-2020
FDA event ID
84687
Recalling firm
Wegmans Food Markets, Rochester, NY
Classification
Class II
Status
Terminated
Recall initiated
9 Jan 2020
FDA classified
21 Jan 2020
Reported
22 Jan 2020
Type
Voluntary: Firm initiated
Customers notified by
Other
Reason category
Undeclared Soy
Product category
Dips & Spreads

Timeline

9 Jan 2020Recall initiated by company
21 Jan 2020Classified by FDA+12 days
22 Jan 2020Published 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

Products contain undeclared soy.

Product as listed by the FDA

Seafood Lobster Dip; Wegmans Lobster Dip, Sold by the lb; Unit size varies; Oven ready tray; Package size varies; Keep Refrigerated or Frozen

Where it was distributed

NY, PA, MD, VA, NJ, MA, NC

MassachusettsMarylandNorth CarolinaNew JerseyNew YorkPennsylvaniaVirginia

Stores named: Wegmans

Questions about this recall

Is Seafood Lobster Dip recalled?

Yes. Wegmans Food Markets recalled Seafood Lobster Dip on 9 Jan 2020. The recall is Class II and its status is Terminated. Recall number F-0545-2020.

Why was it recalled?

Products contain undeclared soy.

Which lots are affected?

All Codes UPC: 2-06332-00000

Where was it sold?

NY, PA, MD, VA, NJ, MA, NC

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 21 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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