Margaret Holmes Mixed Greens 14.5 oz, Distributed by McCall Farms, Effingham, SC
Mccall Farms Inc recalled this product and the FDA reported the enforcement action on 17 December 2014 as Class III. The recall was initiated by the firm. Swollen Cans; Firm received complaints of illnesses due to consumption of recalled products.

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
- Margaret Holmes Mixed Greens 14.5 oz, Distributed by McCall Farms, Effingham, SC
- Reason for recall
- Swollen Cans; Firm received complaints of illnesses due to consumption of recalled products.
- Recalling firm
- Mccall Farms Inc
- Firm location
- Effingham, South Carolina, United States
- Classification
- Class III
- Status
- Terminated
- Recall number
- F-0702-2015
- Quantity
- 1,843 cases (12/14.5oz can per case)
- Distribution
- DC, GA, MD, NC, NJ, SC, PA, TN and VA.
- Initiated
- 22 August 2014
- Reported by FDA
- 17 December 2014
- Terminated
- 23 January 2017
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- Can Code: F13EX
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class III means the FDA judged that the product was unlikely to cause harm but violated FDA labelling or manufacturing regulation. 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 2.4 years, from 22 August 2014 to termination on 23 January 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 9 states, and the FDA published the enforcement report 4 months after the firm began the recall.
- Recalls of fresh produce run a median of 7 months, so this one was longer 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: District of Columbia, Georgia, Maryland, North Carolina, New Jersey, South Carolina, Pennsylvania, Tennessee, Virginia. 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
Spoilage and mould
A spoilage recall means the food degraded before its date: mould growth, unintended fermentation, swelling or rancidity, usually traced to a seal, a formulation or a storage temperature.
A preventive controls plan covers spoilage 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 117.93
- Warehousing and distribution: storage and transport under conditions that protect food against contamination and against deterioration of the food and its container.
- 21 CFR 117.80(b)(3)
- Time and temperature: holding food at temperatures that do not allow microorganisms to grow, and for no longer than the process allows.
Filed under fresh produce. A product can sit in more than one.
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 Mccall Farms Inc
The FDA opens one enforcement record per product code, so several of these are frequently one recall event.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2018-05-09 | Happy Harvest Leaf Spinach; Net Wt. 13.5 oz (383g); Ingredients: Spinach, Water, Salt. Distributed by Aldi Inc. Batavia, IL 60510; Product of USA; Manufactured In A Facility That Processes Peanuts and Soy. May Contain Peanuts and Soy. Packaged in a steel 2-piece can. | Mccall Farms Inc | Canned spinach is being recalled due to the potential to contain boiled peanuts instead of spinach. | Class I |
| 2016-07-06 | Piggly Wiggly, Yellow Cut Corn, Net Wt 32oz (2 lbs), 907g bags, Distributed by Piggly Wiggly LLC, Keene, NH 03431. | Mccall Farms Inc | Possible Listeria monocytogenes contamination. | Class I |
| 2014-12-17 | Margaret Holmes, Turnip Greens, 14.5 oz, Distributed by McCall Farms, Effingham, SC | Mccall Farms Inc | Swollen Cans; Firm received complaints of illnesses due to consumption of recalled products. | Class III |
All 4 records for Mccall Farms Inc
All 2014 recalls · All FDA food recall data
21 CFR 117.93 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.