Recall record at a glance
| Official record | F-1664-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class III |
| FDA record status | Terminated |
| Recalling firm | Orca Bay Foods LLC |
| Report date | Aug 1, 2018 |
| Recall initiation date | Jun 20, 2018 |
| Quantity | 17 cases / 544 lb / 272 units |
| Location | Renton, WA, United States |
Official product description
Consumer Packaging: WELLSLEY FARM WILD CAUGHT MAHI-MAHI LOINS, UPC: 8 88670 00983 3, plastic 2lb retail bag, Keep Frozen. Master Carton: BJ s Wholesale Club Wild Mahi Mahi Loins Skinless Bone Out 16/2Lb. VP Bags. NET WT. 32 LB. Item Code: 32272, UPC: 0 29714 32727 2. Product of Taiwan.
Why the product was recalled
Product is decomposed.
Distribution information
Retail product distributed in FL and NC Wholesale product distributed in MD and FL
How to read the classification
FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement 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.