Hot Salsa sold under the following sizes and brands: 1. Parkers Farm or Parkers label in…
Parkers Farm Inc recalled this product and the FDA reported the enforcement action on 9 July 2014 as Class II. The recall was initiated by the firm. Parkers Farm is recalling cheese and salsa products that may be contaminated with Listeria monocytogenes. This action is being taken as a precaution in response to testing conducted by the Minnesota Department of Agriculture.
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
Hot Salsa sold under the following sizes and brands: 1. Parkers Farm or Parkers label in 16 ounce (51205) container with snap on lid.
Reason for recall
Parkers Farm is recalling cheese and salsa products that may be contaminated with Listeria monocytogenes. This action is being taken as a precaution in response to testing conducted by the Minnesota Department of Agriculture.
Five things about this record are not in the record itself, and each one changes how it should be read.
Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. 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 8 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 8 separate recalls, which almost every published figure does, overstates it by a factor of 8. 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 8 of them.
The recall ran for 16 months, from 5 June 2014 to termination on 20 October 2015. 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 5 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 longer 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: Wisconsin, Indiana, Texas, Illinois, Minnesota. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
Listeria monocytogenes is a bacterium that grows at refrigeration temperature, which is why it dominates recalls of ready-to-eat foods that are never cooked again before they are eaten.
A preventive controls plan covers Listeria 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)(3)
Sanitation controls: the controls on cleaning food-contact surfaces and on preventing cross-contact and cross-contamination from insanitary objects, people and equipment.
21 CFR 117.165(a)(3)
Environmental monitoring: testing the processing environment for an environmental pathogen, required when a ready-to-eat food is exposed to the environment before packaging.
21 CFR 117.150
Corrective actions: what a facility does when a preventive control was not properly implemented, including identifying and correcting the problem and evaluating the food for safety.
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.
Parkers Farm is recalling cheese and salsa products that may be contaminated with Listeria monocytogenes. This action is being taken as a precaution in response to testing conducted by the Minnesota Department of Agriculture.
Parkers Farm is recalling cheese and salsa products that may be contaminated with Listeria monocytogenes. This action is being taken as a precaution in response to testing conducted by the Minnesota Department of Agriculture.
Parkers Farm is recalling cheese and salsa products that may be contaminated with Listeria monocytogenes. This action is being taken as a precaution in response to testing conducted by the Minnesota Department of Agriculture.
Parkers Farm is recalling cheese and salsa products that may be contaminated with Listeria monocytogenes. This action is being taken as a precaution in response to testing conducted by the Minnesota Department of Agriculture.
Parkers Farm is recalling cheese and salsa products that may be contaminated with Listeria monocytogenes. This action is being taken as a precaution in response to testing conducted by the Minnesota Department of Agriculture.
Parkers Farm is recalling cheese and salsa products that may be contaminated with Listeria monocytogenes. This action is being taken as a precaution in response to testing conducted by the Minnesota Department of Agriculture.
Parkers Farm is recalling cheese and salsa products that may be contaminated with Listeria monocytogenes. This action is being taken as a precaution in response to testing conducted by the Minnesota Department of Agriculture.
21 CFR 117.135(c)(3) 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.
Recall 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.
