Food Club Garlic Powder, 5.37 ounce bottles, 12 bottles per case. " Best 324A0 C By NOV…
B&G Foods North America, Inc recalled this product and the FDA reported the enforcement action on 20 January 2021 as Class I. The recall was initiated by the firm. B&G Foods, Inc. has initiated a recall because their garlic powder mistakenly had bacon-flavored bits, which contain soy, an allergen undeclared on the garlic powder labels.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Food Club Garlic Powder, 5.37 ounce bottles, 12 bottles per case. " Best 324A0 C By NOV 19 22 / Best 325A0 By NOV 20 22
- Reason for recall
- B&G Foods, Inc. has initiated a recall because their garlic powder mistakenly had bacon-flavored bits, which contain soy, an allergen undeclared on the garlic powder labels.
- Recalling firm
- B&G Foods North America, Inc
- Firm location
- Parsippany, New Jersey, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-0203-2021
- Quantity
- 1301 Cases
- Distribution
- The product was disturbed to the following states: TX, VA, FL, MN
- Initiated
- 22 December 2020
- Reported by FDA
- 20 January 2021
- Terminated
- 2 November 2021
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- Best 324A0 C By NOV 19 22 Best 325A0 B By NOV 20 22
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class I means the FDA judged a reasonable probability that the product would cause serious health consequences or death. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This record is the only one the FDA opened for its recall event, so it covers a single product code.
- The recall ran for 10 months, from 22 December 2020 to termination on 2 November 2021. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 3 states, and the FDA published the enforcement report 4 weeks after the firm began the recall.
- Recalls of a spice or seasoning run a median of 6 months, so this one was longer than usual for its category. Spices are a low-moisture, globally sourced, minimally processed ingredient that is added after any kill step, which is the combination that makes Salmonella in a spice lot capable of contaminating every product it was blended into.
Named in the distribution pattern: Virginia, Florida, Minnesota. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Undeclared allergens
An undeclared allergen recall means a food contained one of the major allergens and the label did not say so, either because the wrong label was applied or because an ingredient carried an allergen nobody traced.
A preventive controls plan covers an undeclared allergen under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.135(c)(2)
- Food allergen controls: the written preventive controls that keep an allergen out of a food it does not belong in, and that get the allergens present onto the label.
- 21 CFR 101.4
- Ingredient declaration: every ingredient listed by its common name, in descending order of predominance, on the label of a packaged food.
- 21 CFR 117 subpart G
- Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.
The allergens named in this record: soy.
Filed under spices and seasonings. A product can sit in more than one.
Other spices and seasonings recalls for the same reason
These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from B&G Foods North America, Inc
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 13 other records name this firm.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2023-02-15 | Back To Nature Plant Based Snacks Fudge Mint Cookies Net Wt. 6.4 OZ. (181g) UPC code: 819898011025 | B&G Foods North America, Inc | Cookies may contain undeclared peanut residue. | Class III |
| 2022-04-20 | Back to Nature Cheddalicious Cheese Flavored Crackers 6 oz.. UPC: 8-19898-01491-0 6 cartons per case | B&G Foods North America, Inc | Undeclared egg and milk due to mispackaging | Class I |
| 2021-10-20 | Tone s Taco Seasoning Blend, Plastic Bottles / 12 bottles per case with best by dates of SEPT 03 24 and SEPT 06 24, due to the | B&G Foods North America, Inc | Product was recalled due to the presence of undeclared wheat. | Class I |
| 2020-11-18 | Back to Nature Organic Rosemary & Olive Oil Stoneground Wheat Crackers, NET WT 6 oz (170g)., UPC: 8-19898-01015-8 | B&G Foods North America, Inc | B&G Foods initiated a recall of Back to Nature Organic Rosemary & Olive Oil Stoneground Wheat Crackers, 6 oz. with a best by date of APR 25 2021, because package may be filled with peanut butter cookies, which contain peanut, which is not declared on the label. | Class I |
| 2020-09-16 | Back to Nature, Organic Rosemary and Olive Oil Stoneground Wheat Cracker, 6 oz. foil bag inside paper carton, 6 packages per case . | B&G Foods North America, Inc | The product contains undeclared milk. | Class II |
| 2019-03-20 | Victoria Marinara Sauce, 40 oz. (2.5 lb) 1133g, 6Jars / Case | B&G Foods North America, Inc | Product may contain undeclared cashews. | Class I |
| 2014-12-24 | Ortega Taco Sauce - Hot 8 oz, UPC 39000-00891, 16 oz. UPC 41501-01895. | B&G Foods North America, Inc | Specific Ortega Brand Taco Seasoning, Taco Sauce, Taco Dinner Kits, and Enchilada Sauce, and Las Palmas brand Taco Seasoning and Taco Sauce products are being recalled because one or more of the spice ingredients may contain peanuts and almonds. | Class I |
| 2014-12-24 | Ortega Green Taco Sauce - Mild 8 oz, UPC 41501-00897, 16 oz. UPC 41501-00907. | B&G Foods North America, Inc | Specific Ortega Brand Taco Seasoning, Taco Sauce, Taco Dinner Kits, and Enchilada Sauce, and Las Palmas brand Taco Seasoning and Taco Sauce products are being recalled because one or more of the spice ingredients may contain peanuts and almonds. | Class I |
| 2014-12-24 | Ortega Enchilada Sauce 8 oz., UPC 41501-00898 | B&G Foods North America, Inc | Specific Ortega Brand Taco Seasoning, Taco Sauce, Taco Dinner Kits, and Enchilada Sauce, and Las Palmas brand Taco Seasoning and Taco Sauce products are being recalled because one or more of the spice ingredients may contain peanuts and almonds. | Class I |
| 2014-12-24 | Ortega 40% Less Sodium Taco Seasoning 1.25 oz., UPC 41501-00824 | B&G Foods North America, Inc | Specific Ortega Brand Taco Seasoning, Taco Sauce, Taco Dinner Kits, and Enchilada Sauce, and Las Palmas brand Taco Seasoning and Taco Sauce products are being recalled because one or more of the spice ingredients may contain peanuts and almonds. | Class I |
All 14 records for B&G Foods North America, Inc
All 2021 recalls · All FDA food recall data
21 CFR 117.135(c)(2) is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.