Natural Grocers brand Organic Garlic Powder. Natural Grocers brand Organic Garlic…
Vitamin Cottage Natural Food Markets, Inc. recalled this product and the FDA reported the enforcement action on 1 April 2015 as Class I. The recall was initiated by the firm. Vitamin Cottage Natural Food Markets, Inc. is recalling two lots of Natural Grocers brand Organic Garlic Powder because it has the potential to be contaminated with Salmonella.
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
- Natural Grocers brand Organic Garlic Powder. Natural Grocers brand Organic Garlic Powder. Packaged in Zip-Lock-type plastic bags, labeled by random weight, average 0.28 lb. per package, distributed in 25 lb. cases. Packed by Vitamin Cottage Natural Grocers, Inc., Lakewood, CO.
- Reason for recall
- Vitamin Cottage Natural Food Markets, Inc. is recalling two lots of Natural Grocers brand Organic Garlic Powder because it has the potential to be contaminated with Salmonella.
- Recalling firm
- Vitamin Cottage Natural Food Markets, Inc.
- Firm location
- Lakewood, Colorado, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-1580-2015
- Quantity
- 7602 bags
- Distribution
- Distributed to stores in Colorado, Arizona, New Mexico, Texas, Oklahoma, Missouri, Kansas, Nebraska, Utah, Wyoming, Montana, Idaho, Oregon, Washington, Nevada, Arkasas. No distribution to U.S. Defense Supply, VA, or foreign countries.
- Initiated
- 11 February 2015
- Reported by FDA
- 1 April 2015
- Terminated
- 7 January 2016
- Firm notified by
- Product codes
- Julian Packed on Date: 61-15, 40-15, 20-15, 351-14, 006-15, 316-14, 329-14, 288-14, 301-14, 275-14, 267-14, 252-14, 237-14
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 11 months, from 11 February 2015 to termination on 7 January 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 1 state, and the FDA published the enforcement report 7 weeks after the firm began the recall.
- Recalls of a dietary supplement run a median of 15 months, so this one was shorter than usual for its category. Dietary supplements are regulated under their own good manufacturing practice rule, 21 CFR part 111, and they are the only food category where the dominant recall reason is an ingredient that was never declared because it is a pharmaceutical.
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 dietary supplements and spices and seasonings. A product can sit in more than one.
Other dietary supplements 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 Vitamin Cottage Natural Food Markets, Inc.
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 8 other records name this firm.
All 9 records for Vitamin Cottage Natural Food Markets, Inc.
All 2015 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.