Recall record at a glance
| Official record | F-2074-2015 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Con Yeager Spice Co |
| Report date | May 6, 2015 |
| Recall initiation date | Jan 6, 2015 |
| Quantity | 388 units |
| Location | Zelienople, PA, United States |
Official product description
BARBECUE BEEF RUB Con Yeager Spice Company, Zelienople, PA 16053; Net Weight: 5lbs and 20 lbs, UPC: 32276; Lot # .209799; Net Weight: 5lbs and 20 lbs; UPC: 32276; Lot #: .209799; Net Weight: 50lbs; UPC: 32276; Lot #: .213909; Net Weight 13.1oz; UPC: 30890; Lot #: .214818; 215778; 218422 Net Weight 3.68oz; UPC: 30923; Lot #: .217082; .217884 and .218374; JACK BELL'S MEATS Kane, PA 16735 Net Weight 13.1oz; UPC: 30890 ; Lot #: .214783; BURNING ASPHALT SAUCES, LLC, Forestville, NY 14062; Net Weight 3.68oz; UPC: 30923; Lot # .217210; .217728; .217210; BUTLER FARM MARKET, Renfrew, PA 16053 Net Weight:13.1oz; UPC: 30890; Lot # .213793; GREAT LAKE BUTCHER SUPPLY, Howell, MI 48843 Net Weight: 13.1oz; UPC: 30890; Lot #.213257; JIMMY P'S BUTCHER SHOP, Naples, FL 34102 Net Weight: 13.1oz; UPC: 30890; Lot # .213483; .217661; LIVINGSTON PACKING CO., Livingston, PA 16134 Net Weight 13.1oz; UPC: 30890; Lot #: .213306; POTTEIGER MEATS, Sherman's Dale, PA 17090 Net Weight 13.1oz; UPC: 30890; Lot #.219779; SCHRADER FARMS MEAT MARKET, Ramulus, NY 14541 Net Weight 13.1oz; UPC: 30890; Lot # .219542; SHERMAN PROVISION, Norton, OH 44203 Net Weight 13.1oz; UPC: 30890; Lot # .213686; THORNE'S, Salem, OH 44480 Net Weight 13.1oz; UPC: 30890; Lot #.213446; TRADER HORN #10, CLARION, PA 16214 Net Weight 13.1oz; UPC: 30890; Lot #: .215475 TRADER HORN #2, BUTLER, PA 16001 Net Weight 13.1oz; UPC: 30890; Lot #: .213757; .218332
Why the product was recalled
Cumin and cumin containing spice mixes may contain undeclared peanuts.
Distribution information
AZ, CO, DE, FL, GA, IL, LA, MD, MI, MT, NC, NJ, NY, OH, OK, PA, SC, TX, VA, WV
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: Letter.
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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