Recall record at a glance
| Official record | F-0033-2021 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Bumble Bee Foods, LLC |
| Report date | Oct 28, 2020 |
| Recall initiation date | Oct 5, 2020 |
| Quantity | 2,415 cases |
| Location | Santa Fe Springs, CA, United States |
Official product description
Solid White Albacore Tuna in Water; Sold under brand names of Bumble Bee and Kirkland Signature: Bumble Bee NET WT 8-7 oz. (198g) Total 56 oz. (3 lbs 8 oz) 1.59 kg); DR WT 8-5.2 oz. (144g_ total 40..8 oz (2 lb 9 oz) (1.15 kg); For Case UPC 86600-23061, the 8 Pack film UPC is 8660023061, can label UPC is 86600-23059 Kirkland Signature NET WT 8-7 oz. (198g) Total 56 oz. (3 lbs 8 oz) 1.59 kg); DR WT 8-5,4 oz (153g) Total 43.2 oz. (2.7 lbs.) (1.22 kg); For Case UPC 9661933523, the 8-Pack film label UPC is UPC 96619-33523, can label UPC is 96619-97781
Why the product was recalled
During labeling, swollen cans of tuna were found. Two UPC codes for product distributed to one customer did not show signs of swelling but was produced on the same shift as cans that did.
Distribution information
CA,MD, NJ
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
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.