HEB Brand Broccoli Florets: 12oz. UPC: 41220975051 32 oz. UPC: 41220975099 HEB Organic…
Mann Packing Company, Inc. recalled this product and the FDA reported the enforcement action on 27 November 2019 as Class I. The recall was initiated by the firm. CFIA notified FDA of positive result for Listeria monocytogenes with various best by dates of Sweet Kale Salad Blend.
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
- HEB Brand Broccoli Florets: 12oz. UPC: 41220975051 32 oz. UPC: 41220975099 HEB Organic Broccoli Florets: 10 oz.UPC: 41220975167 Mann's Brand: 3 lbs. UPC: 10716519000444 - Food Service 3 lbs. UPC: 10716519030083 - Food Service 3 lbs.Broccoli Floret mini: UPC:10716519000642 - Food Service Mann's Broccoli Wokly: 32 oz. UPC: 716519020162 US and Canada 12 oz. UPC: 716519013010 - Canada Mann's Organic - US and Canada 10 oz. UPC: 716519031014 Marketside brand: UPC: 681131328852 32 oz. UPC: 10681131122341 - Food Service 12 oz. UPC: 681131328845 Marketside Organic 12 oz. UPC. 681131161565 Broccoli Wokly: UPC: 681131161565 Signature Farms brand: 28 oz. UPC: 21130984473 12 oz. UPC; 21130983407; 10 oz, UPC: 716519031014 Weis Markets: 12 oz. UPC: 41497235910
- UPC
- 4122097505132
- Reason for recall
- CFIA notified FDA of positive result for Listeria monocytogenes with various best by dates of Sweet Kale Salad Blend.
- Recalling firm
- Mann Packing Company, Inc.
- Firm location
- Salinas, California, United States
- Classification
- Class I
- Status
- Terminated
- Recall number
- F-0252-2020
- Quantity
- Total: 1,286,466 cases - US,. 141,030 cartons Canada
- Distribution
- US and Canada and Japan
- Initiated
- 3 November 2019
- Reported by FDA
- 27 November 2019
- Terminated
- 6 April 2023
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- Best If Enjoyed By date of October 11, 2019 to November 16, 2019
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 58 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 58 separate recalls, which almost every published figure does, overstates it by a factor of 58. 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 58 of them.
- The recall ran for 3.4 years, from 3 November 2019 to termination on 6 April 2023. 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 weeks 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 Mann Packing Company, Inc.
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 103 other records name this firm.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2019-11-27 | Mann's Rainbow Slaw 6 x 12 oz. UPC: 716519013089 - Canada - Mann 6 x 12 oz. UPC: 716519013089 - SS Same UPC. Two films: one for Canada and one for US. Rainbow Salad 6/12 OZ GE UPC: 3003492350 | Mann Packing Company, Inc. | CFIA notified FDA of positive result for Listeria monocytogenes with various best by dates of Sweet Kale Salad Blend. | Class I |
| 2019-11-27 | Mann's Nourish Bowls Cauli Rice Curry 4 x 11 oz. UPC: 716519036897 UPC: 716519036903 - Mann - Canada Signature Farms Cauli Rice Curry 4 x 11 oz. UPC: 021130600526 | Mann Packing Company, Inc. | CFIA notified FDA of positive result for Listeria monocytogenes with various best by dates of Sweet Kale Salad Blend. | Class II |
| 2019-11-27 | Mann's Crave a Bowl Spicy Marinara 6 x 7 oz. UPC:716519040078 - Canada | Mann Packing Company, Inc. | CFIA notified FDA of positive result for Listeria monocytogenes with various best by dates of Sweet Kale Salad Blend. | Class II |
| 2019-11-27 | Mann's Nourish Bowls Bolognese 4 x 11.5 oz. UPC: 716519037054 4 x 11.5 oz. UPC: 716519037061 - Mann Canada | Mann Packing Company, Inc. | CFIA notified FDA of positive result for Listeria monocytogenes with various best by dates of Sweet Kale Salad Blend. | Class II |
| 2019-11-27 | Mann's Nourish Bowls Sweet Potato 4 x 10.5 oz. UPC: 716519036866 - Mann Canada | Mann Packing Company, Inc. | CFIA notified FDA of positive result for Listeria monocytogenes with various best by dates of Sweet Kale Salad Blend. | Class II |
| 2019-11-27 | Mann's Nourish Bowls Thai Noodle 4 x 9.75 oz. UPC: 716519036989 US and Canada | Mann Packing Company, Inc. | CFIA notified FDA of positive result for Listeria monocytogenes with various best by dates of Sweet Kale Salad Blend. | Class I |
| 2019-11-27 | Mann's Nourish Bowls Basil Pesto 4 x 10.75 oz. UPC: 716519037030 4 x 10.75 oz. UPC; 716519037047 - Mann Canada | Mann Packing Company, Inc. | CFIA notified FDA of positive result for Listeria monocytogenes with various best by dates of Sweet Kale Salad Blend. | Class I |
| 2019-11-27 | Mann's Snacking Favorites Cheddar Pretzel Snack Tray 4 x 19 oz. UPC: 716519020445 | Mann Packing Company, Inc. | CFIA notified FDA of positive result for Listeria monocytogenes with various best by dates of Sweet Kale Salad Blend. | Class I |
| 2019-11-27 | Mann's Snacking Favorites Honey Turkey Cheddar Tray 4 x 20.3 oz. UPC: 716519020483 | Mann Packing Company, Inc. | CFIA notified FDA of positive result for Listeria monocytogenes with various best by dates of Sweet Kale Salad Blend. | Class I |
| 2019-11-27 | Mann's Snappy Slaw Blend 8 x 3 lbs. UPC:10716590067350 Food Service | Mann Packing Company, Inc. | CFIA notified FDA of positive result for Listeria monocytogenes with various best by dates of Sweet Kale Salad Blend. | Class I |
All 104 records for Mann Packing Company, Inc.
All 2019 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.