Friday, March 15, 2019

FDA Issues Recall Notice on Flour Recall for Salmonella

After reports of Pillsbury Flour was issued last week, FDA issued an announcement on March 12th, that Hometown Food Company initiated a limited, voluntary retail-level recall on two specific lot codes of its Pillsbury® Unbleached All-Purpose 5 lb Flour (UPC 51500-22241)because it may be contaminated with Salmonella.  There have been no reports of any illnesses associated with this recall. Product is being recalled out of an abundance of caution.

No specific information was provided on how the contamination was detected.

FDA added the reminder that flour is a raw product - "Flour is made from wheat that is minimally processed. Flour should not be considered a ready-to-eat product. It is an ingredient for baked, fried, and cooked products, and these heating processes ensure the safety of flour with proper handling. All surfaces and utensils should be properly cleaned after contact with flour or uncooked dough or batter. Consumers should wash their hands after handling flour or uncooked dough or batter. Consumers should not eat uncooked dough or batter made with raw flour. If you think you became sick from a food containing flour as an ingredient, please call your healthcare provider."

Hometown Food Company Recalls Two Production LOT Codes of Pillsbury® Unbleached All-Purpose 5lb Flour Due to Possible Health Risk
For Immediate Release
March 12, 2019

PR Establishment Recalls Breaded Chicken Patty Product Due to Complaint of Piece of Metal

Puerto Rico establishment, is recalling approximately 35,870 pounds of breaded chicken patty products that may be contaminated with extraneous materials, specifically pieces of metal,  The problem was discovered on March 11, 2019 after the firm received a consumer complaint from a school that received the product.

https://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2019/recall-031-2019-release
Productos La Aguadillana, Inc. Recalls Breaded Chicken Products Due to Possible Foreign Matter Contamination
Class I Recall 
031-2019
Health Risk:High 
Mar 14, 2019

RTE Meat Snacks Recalled Due to Potential Product Tampering

Monogram Meat Snacks, LLC, a Martinsville, Va. establishment, is recalling approximately 191,928 pounds of ready-to-eat pork sausage products that may be adulterated due to possible product contamination, according to the report, "initiated due to product tampering, following the production process."

No further information is available at this time including how it was discovered.

https://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2019/recall-029-2019-release
Monogram Meat Snacks, LLC Recalls Pork Sausage Products Due to Possible Product Contamination
Class I Recall
029-2019 
Health Risk:High 
Mar 13, 2019 

CDC - 2018 Incident of Botulinum Poisoning from Improperly Home Canned Peas

CDC provided an outbreak report from a June of 2018 incident where three women suffered botulinum poisoning after eating homemade potato salad using improperly processed home-canned peas.

According to the report, the woman's freezer had malfunctioned and so decided to rescue the commercially produced frozen peas by canning them.  HOWEVER, Instead of using a pressure canner, she decided to follow a peach recipe that utilizes a water bath canner, and simply substitute the peas for peaches.  When a jar lost vacuum, she refrigerated it and used that to make the potato salad.

From the report, "The patient who prepared the home-canned peas was a novice home canner. She used a peach preserves recipe with a boiling water technique, replacing the peaches with frozen vegetables. The patient was unaware that low-acid foods (e.g., vegetables) must be canned in a pressure canner rather than a boiling water canner to eliminate C. botulinum spores (1). After the jars cooled, the patient correctly checked for jar seal. One of the jars of peas was not sealed, so the patient covered and refrigerated it, and the family consumed the peas in the potato salad."

The women who had arrived at a hospital 4 hours earlier for evaluation for acute nausea, dizziness, blurred vision, slurred speech, ptosis, thick-feeling tongue, and shortness of breath. Two patients developed respiratory failure, requiring intubation and mechanical ventilation in the emergency department, and the third patient was intubated at 7 p.m. that evening. The combination of cranial nerve palsies and respiratory failure in multiple patients suggested botulism, a paralytic illness caused by botulinum neurotoxin (BoNT), most commonly produced by Clostridium botulinum.

As we know, when you have low acid foods, they must be pressure canned in order to destroy any Clostridium botulinum spores.  In peaches, the acidity is high / ph is low (<4.6) and that prevents the spores from growing, so a high heat treatment is needed.  In peas, a low acid food, the acidity is low and the pH is high (>4.6). In this product, the spores survived the milder heat treatment used in the water bath canning, and when the product cooled down, the spores germinated and grew in the peas, producing the deadly neurotoxin.


https://www.cdc.gov/mmwr/volumes/68/wr/mm6810a5.htm?s_cid=mm6810a5_e
Notes from the Field: Botulism Outbreak Associated with Home-Canned Peas — New York City, 2018
Weekly / March 15, 2019 / 68(10);251–252

Ground Turkey Recalled After Linked to 5 Cases of Salmonella Infection

Butterball, LLC, a Mount Olive, N.C. establishment, is recalling approximately 78,164 pounds of raw ground turkey products that may be contaminated with Salmonella Schwarzengrund.  FSIS, CDC, and Wisconsin state agencies have been investigating a multistate outbreak of Salmonella Schwarzengrund illnesses involving 5 case patients from 2 states

https://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2019/recall-030-2019-release
Butterball LLC Recalls Turkey Products Due to Possible Salmonella Schwarzengrund Contamination
Class I Recall 
030-2019
Health Risk: High 
Mar 13, 2019

Monday, March 11, 2019

This Week in Mislabeled Products for Week Ending March 9, 2019

Beef Ravioli Labeled as Chicken with Rice Conagra Brands, Inc., a Milton, Pa. establishment, is recalling approximately 2,871 pounds of chicken and rice products due to misbranding and undeclared allergens - the products may contain milk and wheat, known allergens, which are not declared on the product label. The problem was discovered by the firm after receiving consumer complaints that  bowls of microwave beef ravioli were mislabeled as “chicken with rice & vegetables.”

https://www.fsis.usda.gov/wps/portal/fsis/topics/recalls-and-public-health-alerts/recall-case-archive/archive/2019/recall-025-2019-release
Conagra Brands, Inc. Recalls Chicken and Rice Products Due To Misbranding and Undeclared Allergens
Class I Recall
025-2019
Health Risk:High
Mar 9, 2019

Grocery Stores Report Recall of Flour Due to Potential Salmonella Contamination

According to news reports, two grocery chains are recalling Pillsbury flour in 5lb bags for potential Salmonella contamination. The chains, Publix and Winn Dixie are both in the Southeast US.

FDA has not yet posted a recall on their website, so there is limited information.

Salmonella can be found in flour and becomes an issue when items are undercooked or not cooked (like raw cookie dough) or there is cross contamination in the kitchen when the contaminated flour gets onto ready-to-eat food items.

http://www.fox13news.com/consumer/publix-winn-dixie-recalls-pillsbury-flour-due-to-salmonella-concern
Publix, Winn-Dixie recalls Pillsbury flour due to salmonella concern
By FOX 13 News staff
Posted Mar 11 2019 05:56AM EDT
Updated Mar 11 2019 07:16AM EDT

Saturday, March 9, 2019

One Lot of Organic Bean Sprouts Recalled for Listeria

A Florida establishment is voluntarily recalling Organic Bean Sprouts because it has the potential to be contaminated with Listeria monocytogenes,  This recall was issued after the Florida Department of Agriculture pulled a sample from a store shelf and found Listeria (we assume).  Product was shipped to Whole Foods Markets in Florida and Freedom Fresh (a Miami distributor) on February 18, 2019 and had a sell by date of February 28, 2019, so unlikely to be in Marketplace.

Like many other recalls involving Listeria where only the tested positive lot is recalled,  these recalls are often expanded as it is discovered that the facility did not have adequate controls in place.  For ensuring public health, recalls of these natures should initially begin with a broad recall unless the company can show that they have had adequate controls in place.   Hard to say in this case, unless over this recall is expanded over the next week.

Fullei Fresh Recalls Organic Bean Sprouts Because of Possible Health Risk
For Immediate Release
March 8, 2019

Thursday, March 7, 2019

FDA Release Guidance on Food Defense - Mitigation Strategies to Protect Food Against Intentional Adulteration

The FDA published a draft guidance for food defense titled Mitigation Strategies to Protect Food Against Intentional Adulteration: Guidance for Industry in support of the Prevention of Intentional Adulteration rule. The draft guidance provides ways to meet the requirements in the rule specifically conducting the vulnerability assessment and putting mitigation strategies in place for ‘actionable process steps’ or APS. These APS are defined as “a point, step, or procedure in a food process where a significant vulnerability exists and at which mitigation strategies can be applied and are essential to significantly minimize or prevent the significant vulnerability”.

To summarize the 159 page document - a Food Defense Plan is essentially conducting a HACCP type of analysis where the goal is to find steps in the process where significant vulnerability exists and to put in measures, or the mitigation strategies’ to reduce the vulnerabilities. These vulnerable points are points where there is access to product where the product can then be contaminated.

There is flexibility in how one conducts a vulnerability assessment, but the guidance provides some basic ways. The elements that must be considered include 1) the potential public health impact (e.g., severity and scale) if a contaminant were added, 2) the degree of physical access to the product; and 3) the ability of an attacker to successfully contaminate the product. The analysis must consider an attack by an insider, a person working in the company. The written assessment must document why each step was considered, or not considered, an APS.

For steps designated as an APS, mitigation strategies are put in place. These strategies may limit access to the step, or may reduce the likelihood that someone can contaminate product at that step. Like critical controls points, each mitigation strategy must have monitoring, verification, and corrective action.

While many may ask about facility wide measures – items such as exterior fencing, employee access to the facility and such – these are not included within the plan unless they can be tailored to impact a specific Actionable Process Step. Sure, they are important, but many have these in place already for other purposes and in reality, they are harder for regulators to regulate.