Jose Madrid Salsa in Zanesville, Ohio is voluntarily recalling its Strawberry Mild salsa, packaged in 13oz glass jars, due to an undeclared anchovy allergen. The issue was discovered during a routine inspection conducted by the Ohio Department of Agriculture. There have been no reports of illness involving the product addressed in this recall, however, people who have an allergy or severe sensitivity to anchovy run the risk of a serious or life-threatening allergic reaction if they consume this product. Individuals exhibiting signs or symptoms of foodborne illness or allergies should contact a physician immediately.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/jose-madrid-salsa-issues-voluntary-recall-due-undeclared-anchovy-allergen
Jose Madrid Salsa Issues a Voluntary Recall Due to an Undeclared Anchovy Allergen
Summary
Company Announcement Date: April 14, 2021
FDA Publish Date: April 15, 2021
Product Type:Food & Beverages Gravy/Sauces
Reason for Announcement: Undeclared anchovy
Company Name: Jose Madrid Salsa
Brand Name: Jose Madrid Salsa
Product Description: Strawberry Mild Salsa
Sunday, April 18, 2021
Trader Joe's Supplier Issues Recall for Undeclared Milk Allergens in Tortilla Chips
Snak King Corporation of City of Industry, CA is voluntarily recalling 9 ounce packages of “Trader Joe’s Restaurant Style White Corn Tortilla Chips” with a sell by date of 08/09/21 and 08/10/21 due to a potential of an undeclared milk allergen.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/snak-king-corporation-issues-allergy-alert-undeclared-milk-allergen-trader-joes-restaurant-style
Snak King Corporation Issues Allergy Alert on Undeclared Milk Allergen in Trader Joe’s Restaurant Style White Corn Tortilla Chips - Expanded to Include 8/11/21 Code Date
Summary
Company Announcement Date: April 13, 2021
FDA Publish Date: April 14, 2021
Product Type: Food & Beverages Sanck Food Item
Reason for Announcement: Product may contain undeclared milk
Company Name: Snak King Corporation
Brand Name: Trader Joe’s
Product Description: Restaurant Style White Corn Tortilla Chips
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/snak-king-corporation-issues-allergy-alert-undeclared-milk-allergen-trader-joes-restaurant-style
Snak King Corporation Issues Allergy Alert on Undeclared Milk Allergen in Trader Joe’s Restaurant Style White Corn Tortilla Chips - Expanded to Include 8/11/21 Code Date
Summary
Company Announcement Date: April 13, 2021
FDA Publish Date: April 14, 2021
Product Type: Food & Beverages Sanck Food Item
Reason for Announcement: Product may contain undeclared milk
Company Name: Snak King Corporation
Brand Name: Trader Joe’s
Product Description: Restaurant Style White Corn Tortilla Chips
Recall of Dark Chocolate Walnuts Labeled as Dark Chocolate Espresso Beans
Torn & Glasser of Los Angeles, CA is recalling 7464 units of dark chocolate espresso beans due to an undeclared walnut allergen. The dark chocolate walnuts were mislabeled as “dark chocolate espresso beans”. The recall was initiated after it was discovered that product containing walnuts was packaged in a container that the top label listed Dark Chocolate Espresso Beans and the bottom label listed Dark Chocolate Walnuts. Subsequent investigation indicates that the wrong label was used by Production personnel.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/urgent-torn-glasser-recalls-dark-chocolate-espresso-beans-because-undeclared-walnut-allergen
Urgent: Torn & Glasser Recalls Dark Chocolate Espresso Beans Because of Undeclared Walnut Allergen
Summary
Company Announcement Date: April 13, 2021
FDA Publish Date: April 13, 2021
Product Type: Food & Beverages
Reason for Announcement: Undeclared walnuts
Company Name: Torn & Glasser
Brand Name: Torn & Glasser
Product Description: Dark chocolate espresso beans
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/urgent-torn-glasser-recalls-dark-chocolate-espresso-beans-because-undeclared-walnut-allergen
Urgent: Torn & Glasser Recalls Dark Chocolate Espresso Beans Because of Undeclared Walnut Allergen
Summary
Company Announcement Date: April 13, 2021
FDA Publish Date: April 13, 2021
Product Type: Food & Beverages
Reason for Announcement: Undeclared walnuts
Company Name: Torn & Glasser
Brand Name: Torn & Glasser
Product Description: Dark chocolate espresso beans
Friday, April 16, 2021
Canadian Establishment Recalls RTE Ham Products After FSIS Sampling Finds Salmonella
Olymel S.E.C./L.P., a Quebec, Canada establishment, is recalling approximately 6,804 pounds of ready-to-eat (RTE) ham products that may be contaminated with Salmonella enteritidis. The problem was discovered when FSIS collected a routine product import sample that confirmed positive for the presence of Salmonella enteritidis. The product subject to recall was determined by the Canadian Food Inspection Agency (CFIA) to be associated with the FSIS positive sample result.
https://www.fsis.usda.gov/recalls-alerts/olymel-s.e.c.l.p.-recalls-ready-eat-ham-products-due-possible-salmonella-enteritidis
Olymel S.E.C./L.P. Recalls Ready-to-Eat Ham Products Due to Possible Salmonella Enteritidis Contamination
WASHINGTON, APRIL 15, 2021 – Olymel S.E.C./L.P., a Quebec, Canada establishment, is recalling approximately 6,804 pounds of ready-to-eat (RTE) ham products that may be contaminated with Salmonella Enteritidis, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
https://www.fsis.usda.gov/recalls-alerts/olymel-s.e.c.l.p.-recalls-ready-eat-ham-products-due-possible-salmonella-enteritidis
Olymel S.E.C./L.P. Recalls Ready-to-Eat Ham Products Due to Possible Salmonella Enteritidis Contamination
WASHINGTON, APRIL 15, 2021 – Olymel S.E.C./L.P., a Quebec, Canada establishment, is recalling approximately 6,804 pounds of ready-to-eat (RTE) ham products that may be contaminated with Salmonella Enteritidis, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.
Monday, April 12, 2021
Dry Cat Food Recall Due to Potential Presence of Salmonella
The J. M. Smucker Co. today announced a limited, voluntary recall of two lots of Meow Mix® Original Choice Dry Cat Food (30LB bag) due to potential salmonella contamination. The Company has received no reports of pet illness or adverse reaction and has issued this recall out of an abundance of caution. The impacted products were sold at select Walmart stores in IL, MO, NE, NM, OK, UT, WI and WY.
No reason was stated for the recall, so it could be through product testing either by the company or by another entity.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/j-m-smucker-co-issues-limited-voluntary-recall-two-lots-meow-mixr-original-choice-dry-cat-food
The J. M. Smucker Co. Issues Limited, Voluntary Recall of Two Lots of Meow Mix® Original Choice Dry Cat Food for Potential Salmonella Contamination
Summary
Company Announcement Date: April 09, 2021
FDA Publish Date: April 12, 2021
Product Type: Animal & Veterinary Pet Food
Reason for Announcement: Potential Salmonella Contamination
Company Name: J. M. Smucker Co.
Brand Name: Meow Mix®
Product Description: Meow Mix® Original Choice Dry Cat Food
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/j-m-smucker-co-issues-limited-voluntary-recall-two-lots-meow-mixr-original-choice-dry-cat-food
The J. M. Smucker Co. Issues Limited, Voluntary Recall of Two Lots of Meow Mix® Original Choice Dry Cat Food for Potential Salmonella Contamination
Summary
Company Announcement Date: April 09, 2021
FDA Publish Date: April 12, 2021
Product Type: Animal & Veterinary Pet Food
Reason for Announcement: Potential Salmonella Contamination
Company Name: J. M. Smucker Co.
Brand Name: Meow Mix®
Product Description: Meow Mix® Original Choice Dry Cat Food
SnoBalls In Wrong Packaging Leads to Recall for Coconut
OH NO....SnoBalls in Chocolate CupCake packaging means that there is undeclared coconut.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/voluntary-recall-hostessr-snoballsr-due-undeclared-allergen
Voluntary Recall of Hostess® SnoBalls® Due to Undeclared Allergen
Summary
Company Announcement Date: April 10, 2021
FDA Publish Date: April 10, 2021
Product Type: Food & Beverages
Reason for Announcement: Undeclared coconut
Company Name: Hostess Brands LLC
Brand Name: Hostess
Product Description: SnoBalls
"Hostess Brands, LLC (”Hostess Brands“) has become aware that certain Hostess® SnoBalls® were inadvertently manufactured in the packaging for Hostess® Chocolate CupCakes and the packaging does not list ”coconut“, an ingredient in SnoBalls®, as an allergen. Hostess Brands is voluntarily recalling the following SnoBalls® manufactured on March 13, 2021."
Hopefully one would recognize the coconut through the clear packaging, but of course we can't count on that.
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/voluntary-recall-hostessr-snoballsr-due-undeclared-allergen
Voluntary Recall of Hostess® SnoBalls® Due to Undeclared Allergen
Summary
Company Announcement Date: April 10, 2021
FDA Publish Date: April 10, 2021
Product Type: Food & Beverages
Reason for Announcement: Undeclared coconut
Company Name: Hostess Brands LLC
Brand Name: Hostess
Product Description: SnoBalls
FDA Releases Investigation Report of 2020 E. coli O157:H7 Outbreak Linked to California Leafy Greens
Here are the bullet points from that report. In a nutshell, cattle in close proximity are the issue and it will take more than the FDA to fix the issue.
- FDA has found that in this and past foodborne illness outbreak investigations "suggest that a likely contributing factor for contamination of leafy greens has been the proximity of cattle."
- FDA "recommends that all growers be aware of and consider adjacent land use practices, especially as it relates to the presence of livestock, and the interface between farmland, rangeland and other agricultural areas, and conduct appropriate risk assessments and implement risk mitigation strategies, where appropriate."
- "The 2020 E. coli O157:H7 outbreak associated with leafy greens represents the latest in a repeated series of outbreaks associated with leafy greens that originated in the Central Coast of California (encompassing Salinas Valley and Santa Maria) growing region."
- FDA "recommends that growers of leafy greens in the California Central Coast Growing Region consider this reoccurring E. coli strain a reasonably foreseeable hazard, and specifically of concern in the South Monterey County area of the Salinas Valley."
- FDA "also recommends that the agricultural community in the California Central Coast growing region work to identify where this reoccurring strain of pathogenic E. coli is persisting and the likely routes of leafy green contamination with STEC."
- FDA "alone cannot fix this issue. Industry leadership and collaboration among growers, processors, retailers, state partners and the broader agricultural community is critical to reducing foodborne illnesses. "
FDA Investigation Report: Factors Factors Potentially Contributing to the Contamination of Leafy Greens Implicated in the Fall 2020 Outbreak of E. coli O157:H7
FDA Leafy Greens STEC Action Plan
https://www.fda.gov/news-events/press-announcements/fda-releases-investigation-report-following-fall-2020-outbreak-e-coli-o157h7-illnesses-linked-leafy
FDA Releases Investigation Report Following Fall 2020 Outbreak of E. coli O157:H7 Illnesses Linked to Leafy Greens
Agency affirms need for new collaborative actions to build on accomplishments in its Leafy Greens Shiga Toxin-Producing E. coli (STEC) Action Plan
FDA Leafy Greens STEC Action Plan
https://www.fda.gov/news-events/press-announcements/fda-releases-investigation-report-following-fall-2020-outbreak-e-coli-o157h7-illnesses-linked-leafy
FDA Releases Investigation Report Following Fall 2020 Outbreak of E. coli O157:H7 Illnesses Linked to Leafy Greens
Agency affirms need for new collaborative actions to build on accomplishments in its Leafy Greens Shiga Toxin-Producing E. coli (STEC) Action Plan
FDA Proposes an Action Plan to Determine Action Levels for Toxic Elements in Baby Food
FDA issued a Statement regarding toxic elements, (primarily lead, arsenic, cadmium, and mercury) in baby foods FDA's goal is "reducing exposure to toxic elements in foods commonly eaten by babies and young children to the lowest possible levels." This comes after a Congressional Subcommittee issued a report on toxic levels of chemicals in baby food (link).
https://www.fda.gov/news-events/press-announcements/fda-releases-action-plan-reducing-exposure-toxic-elements-foods-babies-young-children
FDA Releases Action Plan for Reducing Exposure to Toxic Elements from Foods for Babies, Young Children
For Immediate Release:
April 08, 2021
- Although the FDA’s testing shows that children are not at an immediate health risk from exposure to toxic elements at the levels found in foods, we are starting the plan’s work immediately, with both short- and long-term goals for achieving continued improvements in reducing levels of toxic elements in these foods over time.
- FDA is "sensitive to the fact that requiring levels that are not currently feasible could result in significant reductions in the availability of nutritious, affordable foods that many families rely on for their children. "
- FDA will 1) Evaluate the scientific basis for action levels, 2) Propose Action Levels, 3) Consult with Stakeholder about these propsed action levels, and 4) Finalize the Action Levels.
- It’s important to note that the FDA’s testing shows that children are not at an immediate health risk from exposure to toxic elements at the levels found in foods.
https://www.fda.gov/news-events/press-announcements/fda-releases-action-plan-reducing-exposure-toxic-elements-foods-babies-young-children
FDA Releases Action Plan for Reducing Exposure to Toxic Elements from Foods for Babies, Young Children
For Immediate Release:
April 08, 2021
New York Importer Receives Warning Letter from FDA for FSVP Noncompliance
FDA issued a Warning Letter to IMAD International, LLC Bronx, New York after a remote Foreign Supplier Verification Program (FSVP) inspection as well as an inspection on April 18, 2019. FDA found that this firm was not in compliance with the Foreign Supplier Verification Program (FSVP) regulations by not having a program for the suppliers in which product was purchased.
FDA Warning Letter
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/imad-international-llc-613268-03292021
IMAD International, LLC
MARCS-CMS 613268 — MARCH 29, 2021
FDA Warning Letter
https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/imad-international-llc-613268-03292021
IMAD International, LLC
MARCS-CMS 613268 — MARCH 29, 2021
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