Adams Pantry Basics Ground Cumin Net Wt. 2.82 oz (80 g) UPC: 041313019525; Adams Pantry…
Adams Extract & Spice LLC recalled this product and the FDA reported the enforcement action on 4 March 2015 as Class I. The recall was initiated by the firm. Product may contain undeclared peanut protein.
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
- Adams Pantry Basics Ground Cumin Net Wt. 2.82 oz (80 g) UPC: 041313019525; Adams Pantry Basics Value Size Ground Cumin Net Wt. 6.70 oz (190 g) UPC: 041313019532; Adams Pantry Basics Saver Size Ground Cumin Net Wt. 16 oz (454 g) UPC: 041313023126; No brand name Cumin, Ground 50# Box Item Code: 33325 UPCA: 041313333256 and 25# Box Item Code: 33326 UPCA: 041313333263
- UPC
- 041313019525
- Reason for recall
- Product may contain undeclared peanut protein.
- Recalling firm
- Adams Extract & Spice LLC
- Firm location
- Gonzales, Texas, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-1304-2015
- Quantity
- Unknown
- Distribution
- AL, AR, CA, CO, FL, ID, IL, IN, , KS, KY, LA, MI, MO, MS, NC, NE, NJ, NM, OH, OK, TX, UT, WA
- Initiated
- 26 December 2014
- Reported by FDA
- 4 March 2015
- Terminated
- 5 October 2016
- Firm notified by
- Press Release
- Product codes
- Best Buy Dates:23-Sep-16, 24-Sep-16, 07-Oct-16, 11-Nov-16, 05-Dec-16, 07-Nov-16, 18-Dec-16, 26-Aug-16; Lot: (50# boxes only) P9A53E001, P9A5P1001, P9A69Z001, P9A6N7001, P9A6VB001, P9A7DJ001; Lot: (25 pound boxes only) P9A6M6001
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 is one of 45 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 45 separate recalls, which almost every published figure does, overstates it by a factor of 45. All 45 of them are listed on this page.
- The recall ran for 21 months, from 26 December 2014 to termination on 5 October 2016. 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 23 states, and the FDA published the enforcement report 2 months 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: Alabama, Arkansas, California, Colorado, Florida, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Michigan, Missouri, Mississippi, North Carolina, Nebraska, New Jersey, New Mexico, Ohio, Oklahoma, Texas, Utah, Washington. 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: peanuts.
Filed under spices and seasonings. A product can sit in more than one.
Every product in this recall
The FDA opened 45 enforcement records for this one recall, one per product code. This page carries all of them; the 44 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.
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 Adams Extract & Spice LLC
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 51 other records name this firm.
All 52 records for Adams Extract & Spice LLC
All 2015 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.