Organic Edamame, Brand Columbia River Organics, Net Wt 10 oz, UPC 5711000120 Organic…
CRF Frozen Foods, LLC recalled this product and the FDA reported the enforcement action on 3 August 2016 as Class I. The recall was initiated by the firm. Edamame are recalled because they have the potential to be contaminated with Listeria monocytogenes. Live Smart Edamame have the code format Product of USA 2B6101 02:11 B O Organic Edamame have the code format Best Before: Oct 23 17 S3904 15:08 B Product of USA Signature Kitchens Edamame have the code format Best Before: Oct 23 17 S3904 15:08 B Product of USA Signature Kitchens Shelled Edamame have the code format Best Before: Oct 23 17 S3904 15:08 B Product of USA
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
- Organic Edamame, Brand Columbia River Organics, Net Wt 10 oz, UPC 5711000120 Organic Shelled Edamame, Brand Columbia River Organics, Net Wt 10 oz, UPC 5711000119 Organic Edamame, Brand Organic by Nature, Net Wt 8 oz, UPC 4635800073 Edamame, Brand Live Smart, Net Wt 6 oz, UPC 604369 Edamame, Brand O Organic, Net Wt 16 oz, UPC 7989340179 Edamame, Brand Signature Kitchens, Net Wt 48 oz, UPC 2113009197 Shelled Edamame, Brand Signature Kitchens, Net Wt 16 oz, UPC 2113009092
- UPC
- 5711000120
- Reason for recall
- Edamame are recalled because they have the potential to be contaminated with Listeria monocytogenes. Live Smart Edamame have the code format Product of USA 2B6101 02:11 B O Organic Edamame have the code format Best Before: Oct 23 17 S3904 15:08 B Product of USA Signature Kitchens Edamame have the code format Best Before: Oct 23 17 S3904 15:08 B Product of USA Signature Kitchens Shelled Edamame have the code format Best Before: Oct 23 17 S3904 15:08 B Product of USA
- Recalling firm
- CRF Frozen Foods, LLC
- Firm location
- Pasco, Washington, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-1809-2016
- Quantity
- 437,752 lbs
- Distribution
- US nationwide and in Canada & Japan.
- Initiated
- 2 May 2016
- Reported by FDA
- 3 August 2016
- Terminated
- 11 September 2017
- Firm notified by
- Press Release
- Product codes
- All affected products have the best by dates or sell by dates between April 26, 2016 and April 26, 2018. Live Smart Edamame 6oz 604369 Product of USA 2B6101 02:11 B O Organic Edamame 16oz 7989340179 Best Before: Oct 23 17 S3904 15:08 B Product of USA Signature Kitchens Edamame 48oz 2113009197 Best Before: Oct 23 17 S3904 15:08 B Product of USA Signature Kitchens Shelled Edamame 16oz 2113009092 Best Before: Oct 23 17 S3904 15:08 B Product of USA
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 23 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 23 separate recalls, which almost every published figure does, overstates it by a factor of 23. 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 23 of them.
- The recall ran for 16 months, from 2 May 2016 to termination on 11 September 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 FDA published the enforcement report 3 months after the firm began the recall.
- The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.
What this recall was for
Listeria monocytogenes
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 records from CRF Frozen Foods, LLC
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 53 other records name this firm.
All 54 records for CRF Frozen Foods, LLC
All 2016 recalls · All FDA food recall data
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.
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.