Jose Madrid Salsa Strawberry Mild Salsa Recall [US]

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US/Silver Spring: Jose Madrid Salsa, a Zanesville, Ohio establishment, recalls certain batch/lots of Strawberry Mild Salsa from the American marketplace due to suspected Anchovy Fish, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention.

FDA: http://ht.ly/IslQ30rF9Zv

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/jose-madrid-salsa-issues-voluntary-recall-due-undeclared-anchovy-allergen

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Salsa products are subject to this recall:

Panera at Home Lobster Bisque Recall [US]

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US/Silver Spring: Blount Fine Foods, a Fall River, Massachusetts establishment, recalls an estimated 2,987 cases of Panera at Home branded Lobster Bisque Cups from the American marketplace due to undeclared Egg, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention.

FDA: http://ht.ly/A0LU30rF31Y

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/blount-fine-foods-voluntarily-recalls-limited-amount-single-lot-lobster-bisque-due-possible

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Lobster Bisque Cups are subject to this recall:

EU issues 45 Product, Toy & Vehicle Recalls

Belgium/Brussels: The European Union issues Report 15/2021 of its Rapid Alert System containing forty-five (45) consumer, automotive, commercial and industrial-based product recalls, a must-read for parents, caregivers, drivers, health and safety workers, company owners, healthcare workers and others: http://ht.ly/utIL30rEHJy

Direct link: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10003468

Additional information:

Celebrity Extra Lean Imported Ham Recall [US]

US/Washington: Olymel SEC/LP, a St-Hyacinthe, Quebec establishment, recalls an estimated 6,804 pounds of ready-to-eat (“RTE”) Celebrity branded Extra Lean Imported Ham 98% Fat Free products from the American marketplace due to suspected Salmonella Enteritidis contamination and consequential risks of Gram-negative bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

USDA: http://ht.ly/UhUn30rEVJI

Direct link: https://www.fsis.usda.gov/recalls-alerts/olymel-s.e.c.l.p.-recalls-ready-eat-ham-products-due-possible-salmonella-enteritidis

Additional information:
The United States Department of Agriculture (“USDA”) reports the following Imported Ham products were packaged on November 5, 2020 and are subject to this recall:

Lake Champlain Mr. Goodtime Chocolate Bunny Recall [US]

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US/Silver Spring: Lake Champlain Chocolates (“LCC”), a Burlington, Vermont establishment, recalls certain batch/lots of Mr. Goodtime Chocolate Bunny Confections from the American marketplace due to undeclared Almond Nuts, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention.

FDA: http://ht.ly/zq0R30rEMEk

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/lake-champlain-chocolates-voluntarily-recalls-mr-goodtime-bunny-best-date-11202021-undeclared

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Chocolate Confectionery products are subject to this recall:

Kroger Dark Chocolate Espresso Beans Recall [US]

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US/Silver Spring: Torn & Glasser, a Los Angeles, California establishment, recalls an estimated 7464 units of Kroger Dark Chocolate Espresso Beans from the American marketplace due to suspected mispackaging/mislabeling and consequential risks of undeclared Walnuts, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention.

FDA: http://ht.ly/wM7m30rEETJ

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/urgent-torn-glasser-recalls-dark-chocolate-espresso-beans-because-undeclared-walnut-allergen

Kroger Dark Chocolate Espresso Beans Recall [US]

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Espresso Bean products are subject to this recall:

Trader Joe’s Corn Tortilla Chip Recall [US]

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US/Silver Spring: Snak King Corporation, a City of Industry, California establishment, recalls certain batch/lots of Trader Joe’s Restaurant Style White Corn Tortilla Chips from the American marketplace due to undeclared Milk, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention.

FDA: http://ht.ly/TSCQ30rEw88

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/snak-king-corporation-issues-allergy-alert-undeclared-milk-allergen-trader-joes-restaurant-style

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Tortilla Chip products are subject to this recall:

Sainsbury’s Taste the Difference Medjool Dates Recall [UK]

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UK/London: Sainsbury’s Supermarkets Ltd (“Sainsbury’s”) a London, England establishment, recalls certain batch/lots of Sainsbury’s Taste the Difference Medjool Dates from the British marketplace due to suspected Hepatitis A contamination and consequential risks of viral infection, severe illness and/or possible life-changing complications, all serious health hazards.

FSA: http://ht.ly/l5bQ30rEr9i

Direct link: https://www.food.gov.uk/news-alerts/alert/fsa-prin-25-2021

Additional information:
The UK Food Standards Agency (“FSA”) reports the following Medjool Dates are subject to recall:

Premium OrgaZen & Ginseng Power Supplement Recall [US]

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US/Silver Spring: NS NY Distributor Inc. recalls all current batch/lots of Premium OrgaZen 7000 and Ginseng Power 5000 Dietary Supplements from the American marketplace due to reported undeclared Sildenafil and Tadalafil, two FDA approved drugs for the treatment of Male Erectile Dysfunction (“ED”), Benign Prostatic Hyperplasia (“BPH”) and certain other medical conditions and in a class of drugs called Phosphodiesterase (“PDE-5”) Inhibitors with consequential risks of dangerous low blood pressure, injury and possible life-changing complications, all serious health and safety hazards.

FDA: http://ht.ly/tLLD30rEos8

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ns-ny-distributor-inc-issues-voluntary-nationwide-recall-premium-orgazen-7000-and-ginseng-power-5000

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Dietary Supplement products are subject to this recall:

Hostess SnoBall Cupcake Recall [US]

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US/Silver Spring: Hostess Brands, LLC (”Hostess Brands“), a Lenexa, Kansas establishment, recalls certain batch/lots of Hostess SnoBalls Cupcakes from the American marketplace due to suspected mislabeling/mispackaging and consequential undeclared Coconut, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention.

FDA: http://ht.ly/KBRx30rEhFQ

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/voluntary-recall-hostessr-snoballsr-due-undeclared-allergen

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Cupcake products are subject to this recall:

EU issues 17 Product, Toy & Vehicle Recalls

Belgium/Brussels: The European Union issues Report 14/2021 of its Rapid Alert System containing seventeen (17) consumer, automotive, commercial and industrial-based product recalls, a must-read for parents, caregivers, drivers, health and safety workers, company owners, healthcare workers and others: http://ht.ly/uoYh30rE2Ht

Direct link: https://ec.europa.eu/safety-gate-alerts/screen/webReport/detail/10000041

Additional information:

Nature’s Promise & Wegman Ground Turkey Warning [US]

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US/Washington: The US Department of Agriculture’s Food Safety and Inspection Service (“FSIS”), a statutory regulatory and food safety authority, issues public health alert and warning against the consumption of approximately 211,406 pounds of Raw Ground Turkey Products, produced by Plainville Brands, LLC, a New Oxford, Pennsylvania establishment, due to concerns the products may have caused Salmonella Hadar illness, a Gram-negative bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

USDA: http://ht.ly/RVzn30rEaqJ

Direct link: https://www.fsis.usda.gov/recalls-alerts/fsis-issues-public-health-alert-raw-ground-turkey-products-linked-salmonella-hadar

Additional information:
The United States Department of Agriculture (“USDA”) reports the following Nature’s Promise Free branded, Plainville Farms branded and Wegman branded Ground Turkey Products were thought to have been produced on dates ranging from December 18, 2020 to December 29, 2020 and are subject to this recall:

Glutenull Goji Berries and Chocolate Cookie Recall [US]

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US/Silver Spring: Glutenull Bakery, a Port Coquitlam, British Columbia, establishment, recalls certain batch/lots of Goji Berries and Chocolate Cookies from the American marketplace due to undeclared Milk, a known allergen, source of dietary intolerance and possible trigger of Anaphylaxis, a serious and potential fatal situation, requiring immediate medical intervention.

FDA: http://ht.ly/bAv330rDYuG

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/glutenull-bakery-issues-allergy-alert-undeclared-milk-goji-berries-and-chocolate-cookies

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Cookies are subject to this recall:

Nuri Shogun-X 7000, 69MODE & Thumbs Up 7 Supplements

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US/Silver Spring: Nuri Trading, a Newton, New Jersey, establishment, recalls all current batch/lots of Shogun-X 7000 Supplement Capsules, 69MODE Blue 69 Supplement Capsules, Thumbs Up 7 (Black) 25K Supplement Capsules and Thumbs Up 7 (White) 11K Supplement Capsules from the American marketplace due to reported undeclared Sildenafil, Tadalafil and Vardenafil, three (3) FDA approved drugs for the treatment of Male Erectile Dysfunction (“ED”), Benign Prostatic Hyperplasia (“BPH”) and certain other medical conditions and in a class of drugs called Phosphodiesterase (“PDE-5”) Inhibitors with consequential risks of dangerous low blood pressure, injury and possible life-changing complications, all serious health and safety hazards.

FDA: http://ht.ly/4jiJ30rDJ1l

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/nuri-trading-llc-issues-voluntary-nationwide-recall-shogun-x-7000-thumbs-7-black-25k-thumbs-7-white

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Dietary Supplement products are subject to this recall:

Ummzy Krazy Night, Shogun-X & Thumbs Up Recall [US]

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US/Silver Spring: Ummzy LLC, a Palisades Park, New Jersey establishment, recalls all current batch/lots of Krazy Night Dietary Supplement Capsules, Shogun-X 15000 mg Dietary Supplement Capsules and Thumbs Up 7 Red 70K Dietary Supplement Capsules from the American marketplace due to reported undeclared Sildenafil, Tadalafil and Vardenafil, three (3) FDA approved drugs for the treatment of Male Erectile Dysfunction (“ED”), Benign Prostatic Hyperplasia (“BPH”) and certain other medical conditions and in a class of drugs called Phosphodiesterase (“PDE-5”) Inhibitors with consequential risks of dangerous low blood pressure, injury and possible life-changing complications, all serious health and safety hazards.

FDA: http://ht.ly/TkLw30rDCMy

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ummzy-llc-issues-voluntary-nationwide-recall-thumbs-7-red-70k-shogun-x-15000mg-and-krazy-night-due

Additional information:
The US Food and Drug Administration (“FDA”) reports the following Dietary Supplement products are subject to this recall: