FDA Recall United States TerminatedTerminated: April 26, 2018Historical recordClass II
Wegmans Food Markets, Inc.
- Product
- Wegmans Ready To Cook Lobster & Shrimp Steam Pot, Sold by th…
- Published
- February 7, 2018
- Distribution
- Multiple states
Wegmans Food Markets, Inc. Recall: Products may contain undeclared soy lecithin. - F-0755-2018
United States
TerminatedClass II
- Company
- Wegmans Food Markets, Inc.
- Product
- Wegmans Ready To Cook Shrimp Scampi, 6 oz. UPC: 2-16151-0000…
- Recall date
- January 19, 2018
- Terminated
- April 26, 2018
- Source
- FDA
Reason for recall
Products may contain undeclared soy lecithin.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Wegmans Ready To Cook Shrimp Scampi, 6 oz. UPC: 2-16151-00000 | 2-16151-00000 | 618 packages (total for all products) | Only packages with use or freeze by dates from January 11th to January 23rd are affected. |
Distribution
- NY
- PA
- NJ
- MD
- VA
- MA
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0755-2018
- Event ID
- 78984
- Status
- Terminated
- Classification
- Class II
- Company
- Wegmans Food Markets, Inc.
- Product description
- Wegmans Ready To Cook Shrimp Scampi, 6 oz. UPC: 2-16151-00000
- Quantity
- 618 packages (total for all products)
- Reason
- Products may contain undeclared soy lecithin.
- Recall initiation date
- January 19, 2018
- Report date
- February 7, 2018
- Classification date
- Not published in this source record
- Termination date
- April 26, 2018
- Distribution pattern
- NY, PA, NJ, MD, VA, MA
- UPC, lot, and code information
- UPC 2-16151-00000; Only packages with use or freeze by dates from January 11th to January 23rd are affected.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 78984 with 3 other product entries in Public Health Trace.
FDA Recall United States TerminatedTerminated: April 26, 2018Historical recordClass II
Wegmans Food Markets, Inc.
- Product
- Wegmans Ready To Cook Tom Tom Shrimp with Sauce, 11 oz UPC:…
- Published
- February 7, 2018
- Distribution
- Multiple states
FDA Recall United States TerminatedTerminated: April 26, 2018Historical recordClass II
Wegmans Food Markets, Inc.
- Product
- Wegmans Ready To Cook Garlic Parmesan Tilapia, Single, 5 oz…
- Published
- February 7, 2018
- Distribution
- Multiple states
Responsible company: Wegmans Food Markets, Inc.
Other recalls from Wegmans Food Markets, Inc.
FDA Recall United States TerminatedTerminated: February 11, 2026Historical recordClass I
Wegmans Food Markets, Inc.
- Product
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- Published
- December 31, 2025
- Distribution
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FDA Recall United States TerminatedTerminated: April 21, 2026Historical recordClass I
Wegmans Food Markets, Inc.
- Product
- Large Ultimate Fresh Fruit Topped Cheesecake, Net Wt. 55 oz…
- Published
- October 29, 2025
- Distribution
- VA, MD, NC, D.C.
FDA Recall United States TerminatedTerminated: April 21, 2026Historical recordClass I
Wegmans Food Markets, Inc.
- Product
- Wegmans Brulee Cheesecake Large, Net Wt. 51 oz. (3.19 lb) (…
- Published
- October 29, 2025
- Distribution
- VA, MD, NC, D.C.
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| New York | 1 |
| Pennsylvania | 1 |
| New Jersey | 1 |
| Maryland | 1 |
| Virginia | 1 |
| Massachusetts | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of April 26, 2018.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.