CLASS II Food recall · Reported 8 Nov 2017 · FDA Enforcement Report
Wegmans Single Cheese Cannoli recalled by Wegmans Food Markets
Wegmans Food Markets is recalling Wegmans Single Cheese Cannoli, distributed in Massachusetts, Maryland, New Jersey, New York, Pennsylvania, Virginia. The recall was initiated on 26 Oct 2017 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-0106-2018
- FDA event ID
- 78388
- Recalling firm
- Wegmans Food Markets, Rochester, NY
- Brand
- Wegmans Single
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 26 Oct 2017
- FDA classified
- 2 Nov 2017
- Reported
- 8 Nov 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Soy
- Product category
- Cakes & Pastries
Timeline
| 26 Oct 2017 | Recall initiated by company | |
| 2 Nov 2017 | Classified by FDA | +7 days |
| 8 Nov 2017 | Published 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
Products contain undeclared soy lecithin
Product as listed by the FDA
Wegmans Single Cheese Cannoli, 2 oz. UPC: 0-77890-17163
Where it was distributed
NJ, NY, MD, MA, PA, VA,
MassachusettsMarylandNew JerseyNew YorkPennsylvaniaVirginia
Stores named: Wegmans
Questions about this recall
Is Wegmans Single Cheese Cannoli recalled?
Yes. Wegmans Food Markets recalled Wegmans Single Cheese Cannoli on 26 Oct 2017. The recall is Class II and its status is Terminated. Recall number F-0106-2018.
Why was it recalled?
Products contain undeclared soy lecithin
Which lots are affected?
Sold prior to October 26, 2017
Where was it sold?
NJ, NY, MD, MA, PA, VA,
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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