Recall record at a glance
| Official record | F-0378-2016 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Skipanon Brand Seafoods LLC |
| Report date | Dec 16, 2015 |
| Recall initiation date | Oct 9, 2015 |
| Quantity | approximately 57,000 cans total |
| Location | Warrenton, OR, United States |
Official product description
Albacore Tuna in gold pouches with stick-on label reading in part: ***SKIPANON BRAND SEAFOOD ALBACORE TUNA***INGREDIENTS: Albacore Tuna, Sea Salt. NET WT. 48 OZ. ***" UPC: 58071 00148 Code on pouch beginning with OCK TUNA 3#. Label has green, yellow and blue background with multiple color lettering. Canned Albacore Tuna with paper label reading in part: ***SKIPANON BRAND SEAFOOD ALBACORE TUNA***Ingredients: Albacore Tuna, Sea Salt. NET WT. 66.5 OZ. (1885g)***" UPC: 58071 00144 Can code beginning with OCK. Label has a yellow background and a blue strip on the bottom. Lettering is in multiple colors. Canned Albacore Tuna with paper label reading in part: ***SKIPANON BRAND SEAFOOD ALBACORE TUNA***INGREDIENTS: Albacore Tuna, Sea Salt. NET WT. 6 OZ. (170g)***" UPC: 58071 00117 Can code beginning with OCK. Label has a yellow background and a blue strip on the bottom. Lettering is in multiple colors. Canned Albacore Tuna 6oz, 7oz, and 64oz cans without labeling, salt added, distributed as brites. Can code beginning with OCK.
Why the product was recalled
All cans and pouches of Skipanon Brand seafood, including tuna products are being recalled due to lack of documentation and possible under-processed product. Under-processed seafood could lead to contamination with Clostridium botulinum.
Distribution information
No Foreign Consignees No VA or DoD Consignees. Distributed to Michigan, Nevada, Oregon, and Washington and sold to internet customers nationwide from the website skipanonbrand.com.
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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
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
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