Cranberry Health Mix: America Choice, 16 oz. Plastic Pouch, UPC: 75480779046; Aurora…
Aurora Products, Inc. recalled this product and the FDA reported the enforcement action on 20 May 2015 as Class I. The recall was initiated by the firm. 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
- Cranberry Health Mix: America Choice, 16 oz. Plastic Pouch, UPC: 75480779046; Aurora , 9.25 oz. Plastic Cup, UPC: 65585200288; Aurora , 10.0 oz. Pillow Pouch, UPC: 65585200826; Aurora, 16.0 oz. Plastic Pouch, UPC: 65585200827, Aurora , 18 oz. Plastic Pouch , NO UPC; Aurora , 21 oz. Plastic Cup, UPC: 65585200585; Aurora , 4.5 oz. Single Serve, UPC: 65585200208; Aurora, 1.35 oz. Single Serve, UPC: 65585200574; Aurora Bulk, NO UPC; Belmont Market , 9.25 oz. Plastic Cup, UPC: 65585200288; Belmont Market, 21 oz. Plastic Cup, UPC: 65585200585; Citarella Brand Products, 9.25 oz. Plastic Cup, UPC: 79084505949; Citarella Brand Products, Bulk, NO UPC; Food Emporium Brand Products, 7.5 oz. Gift Bag, UPC: 1119079044; Food Emporium Brand Products, 21 oz. Plastic Cup, UPC: 1119079010; Gauls Market Brand Products, 9.25 oz. Plastic Cup, UPC: 65585200288, Gauls Market Brand Products, 21 oz. Plastic Cup, UPC: 65585200585; Giant Carlisle Food Store, 21 oz. Plastic Cup, UPC: 68826713692; Giant Carlisle Food Store, 9.25 oz. Plastic Cup, UPC: 68826714713; Giant of Maryland, 21 oz. Plastic Cup, UPC: 68826713692; Giant of Maryland, 9.25 oz. Plastic Cup, UPC: 68826714713; Gourmet Garage, 9.25 oz. Plastic Cup, UPC: 79084505949; Gourmet Garage, 21 oz. Plastic Cup, UPC: 79084505603; Green Hills Market, 9.25 oz. Plastic Cup, UPC: 65585200288; Green Hills Market, 21 oz. Plastic Cup, UPC: 65585200585; Harvest Co Op Market , 9.25 oz. Plastic Cup, UPC: 65585200288; Hurley Ridge 9.25 oz. Plastic Cup, UPC: 65585200288; Hurley Ridge, 21 oz. Plastic Cup, UPC: 65585200585; Lees Market, 9.25 oz. Plastic Cup, UPC: 65585200288; Lees Market, 21 oz. Plastic Cup, UPC: 65585200585; Martins Food, 21 oz. Plastic Cup, UPC: 68826713692; Martins Food, 9.25 oz. Plastic Cup, UPC: 68826714713; Miles Market, 9.25 oz. Plastic Cup, UPC: 65585200288; Stop & Shop, 21 oz. Plastic Cup, UPC: 68826713692; Stop & Shop, 9.25 oz. Plastic Cup, UPC: 68826714713; Union Market , 9.25 oz. Plastic Cup, UPC: 65585200288; Whole Foods Market , 9.25 oz. Plastic Cup, UPC: 65585200288; Whole Foods Market , 21 oz. Plastic Cup, UPC: 65585200585; Wild Acorns , 9.25 oz. Plastic Cup, UPC: 81957401025; Wild Acorns, 16.0 oz. Plastic Pouch, UPC: 81957401114; Wild By Nature Brand Products, 9.25 oz. Plastic Cup, UPC: 65585270288; Windfall Market, 9.25 oz. Plastic Cup, UPC: 65585200288; Hannaford, 9.25 oz. Plastic Cup, 72543994563
- UPC
- 75480779046
- Reason for recall
- Salmonella
- Recalling firm
- Aurora Products, Inc.
- Firm location
- Orange, Connecticut, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-2262-2015
- Quantity
- 124,572.7 lbs
- Distribution
- Product shipped to distributors in the following states: NY, CT, NH, RI, MA, CA, MD, ME, MN, PA and Nationwide through retail stores. Canada: Winners, HomeSense and Marshalls stores Bermuda
- Initiated
- 20 March 2015
- Reported by FDA
- 20 May 2015
- Terminated
- 17 August 2015
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- Best if used by date range: 10/30/15 12/13/15 and 12/16/2015
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 12 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 12 separate recalls, which almost every published figure does, overstates it by a factor of 12. All 12 of them are listed on this page.
- The recall ran for 5 months, from 20 March 2015 to termination on 17 August 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 9 states, and the FDA published the enforcement report 2 months after the firm began the recall.
- Recalls of fresh produce run a median of 7 months, so this one was shorter than usual for its category. Fresh produce is the category where contamination arrives before the facility does: irrigation water, soil amendments and field workers are the routes, and nothing downstream of the farm is a kill step for a product eaten raw.
Named in the distribution pattern: Connecticut, New Hampshire, Rhode Island, Massachusetts, California, Maryland, Maine, Minnesota, Pennsylvania. 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 fresh produce. A product can sit in more than one.
Every product in this recall
The FDA opened 12 enforcement records for this one recall, one per product code. This page carries all of them; the 11 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 fresh produce 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 Aurora Products, Inc.
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 18 other records name this firm.
All 19 records for Aurora Products, 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.