WOOD FARMS Ranch dressing, EX418, NET WT: 6.4 oz, UPC 9172850097
J M Exotic Foods Inc recalled this product and the FDA reported the enforcement action on 25 January 2017 as Class I. The recall was initiated by the firm. Spice blends were manufactured using dried buttermilk which was subsequently recalled due to positive Salmonella results on environmental sampling.
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
- WOOD FARMS Ranch dressing, EX418, NET WT: 6.4 oz, UPC 9172850097
- UPC
- 9172850097
- Reason for recall
- Spice blends were manufactured using dried buttermilk which was subsequently recalled due to positive Salmonella results on environmental sampling.
- Recalling firm
- J M Exotic Foods Inc
- Firm location
- Moody, Alabama, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-1271-2017
- Quantity
- 144 cases of 12 units
- Distribution
- AL and SC
- Initiated
- 21 December 2016
- Reported by FDA
- 25 January 2017
- Terminated
- 17 April 2017
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- Lot Numbers: #16154141 Best By: 06/02/2018; 16175149 Best By: 06/23/2018; 16203143 Best By: 07/21/2018; 16245128 Best By: 09/01/2018; 16294119 Best By: 10/20/2018; 16300120 Best By: 10/26/2018; 16328129 Best By: 11/28/2018
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 2 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 2 separate recalls, which almost every published figure does, overstates it by a factor of 2. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 2 of them.
- The recall ran for 4 months, from 21 December 2016 to termination on 17 April 2017. 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 2 states, and the FDA published the enforcement report 5 weeks after the firm began the recall.
- Recalls of a sauce, dip or condiment run a median of 6 months, so this one was shorter than usual for its category. Sauces and dips sit at the intersection of the acidified foods rule and the allergen rule: an equilibrium pH above 4.6 turns a shelf-stable product into a botulism risk, and the ingredient list is long enough that an allergen is easy to lose.
Named in the distribution pattern: Alabama, South Carolina. 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
Salmonella
Salmonella is a bacterium that survives in low-moisture foods for months, which is why it appears in recalls of products that carry no water for it to grow in: nut butters, spices, flour and dry pet food.
A preventive controls plan covers Salmonella contamination 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)(1)
- Process controls: the controls that apply a treatment, such as a validated kill step, at the point where it reduces the hazard to a safe level.
- 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.
- 21 CFR 117.165(a)(2)
- Product testing: testing as a verification activity, appropriate to the facility, the food and the nature of the preventive control.
Filed under sauces, dips and condiments. A product can sit in more than one.
Other sauces, dips and condiments 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 J M Exotic Foods Inc
The FDA opens one enforcement record per product code, so several of these are frequently one recall event.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2017-03-22 | Ground Turmeric packaged as follows: a) FOOD LOCKER(R) , 16 oz, PHENIX FOOD SERVICE, PHENIX CITY, AL 36867 b) Ground Turmeric, Net Wt. 4 oz., | J M Exotic Foods Inc | The firm received a notice from their supplier that a sample of ground turmeric was tested and found to have elevated levels of lead. | Class I |
| 2017-01-25 | Tupperware, Southwest Chipotle Seasoning, Assaisonnement Chipotle du sud-ouest, NET WT. 2.0 OZ. (56g) | J M Exotic Foods Inc | Spice blends were manufactured using dried buttermilk which was subsequently recalled due to positive Salmonella results on environmental sampling. | Class I |
All 3 records for J M Exotic Foods Inc
All 2017 recalls · All FDA food recall data
21 CFR 117.135(c)(1) 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.