Recall record at a glance
| Official record | F-0614-2017 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | HANDY SEAFOOD Inc. |
| Report date | Dec 14, 2016 |
| Recall initiation date | Nov 22, 2016 |
| Quantity | 71 Cases Distributed to Whole Foods North Atlantic |
| Location | Salisbury, MD, United States |
Official product description
Handy Seafood, Blue Crab Cake Mini, Mini Crab Cakes, 0.5oz per Cake/12 Cakes per Tray, Skin Packed Tray, 12 Trays per Case, 2 Year Shelf Life, Best By Nov 9, 2018.
Why the product was recalled
Handy Seafood states that they are initiating this recall of Blue Crab Cake Mini, Mini Crab Cakes due to Milk (due to Butter in the ingredient statement) and Anchovies (in the Worcestershire Sauce) were not declared in the allergens statement on the package.
Distribution information
Gloucester, MA. (product further distributed by consignee to stores in CT, ME, MA, NH, RI)
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.