Guan’s Enoki Mushroom Recall [US]

Guan’s Enoki Mushroom Recall [US]

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US FlagUS/Silver Spring: Guan’s Mushroom Co., a Commerce, California establishment, recalls certain batch/lots of Enoki Mushroom products from the American marketplace due to suspected Listeria monocytogenes contamination and consequential risks of Gram-positive bacterial infection, severe illness and/or possible life-changing complications, all serious health hazards.

FDA: http://ht.ly/XuMx30rFhP9

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/guans-mushroom-co-recalls-enoki-because-possible-health-risk-0

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

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Jose Madrid Salsa Strawberry Mild Salsa Recall [US]

Jose Madrid Salsa Strawberry Mild Salsa Recall [US]

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US FlagUS/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:

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Panera at Home Lobster Bisque Recall [US]

Panera at Home Lobster Bisque Recall [US]

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US FlagUS/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:

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Lake Champlain Mr. Goodtime Chocolate Bunny Recall [US]

Mr. Goodtime Chocolate Bunny Recall [US]

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US FlagUS/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:

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Kroger Dark Chocolate Espresso Beans Recall [US]

Torn & Glasser Dark Chocolate Espresso Beans

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US FlagUS/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:

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Trader Joe’s Corn Tortilla Chip Recall [US]

Trader Joe's Restaurant Style White Corn Tortilla Chip Recall [US]

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US FlagUS/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:

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Premium OrgaZen & Ginseng Power Supplement Recall [US]

Premium OrgaZen 7000 and Ginseng Power 5000 Supplements Recall [US]

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US FlagUS/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:

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Hostess SnoBall Cupcake Recall [US]

Hostess SnoBalls Cupakes Recall [US]

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US FlagUS/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:

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Glutenull Goji Berries and Chocolate Cookie Recall [US]

Glutenull Goji Berries and Chocolate Cookie Recall [US]

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US FlagUS/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:

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

Nuri Shogun-X 7000, 69MODE Blue 69, Thumbs Up 7 Supplements [US]

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US FlagUS/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:

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

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

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US FlagUS/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:

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Bit & Bet Thumbs Up 7 Blue 69K Supplement Recall [US]

Bit & Bet Thumbs Up 7 Blue 69K Supplement Capsules

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US FlagUS/Silver Spring: Bit & Bet LLC, a Manassas, Virginia establishment, recalls all batch/lots of Bit & Bet Thumbs Up 7 Blue 69K Supplement Capsules 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/GcCM30rDtk4

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/bit-bet-llc-issues-voluntary-nationwide-recall-thumbs-7-blue-69k-due-presence-undeclared-sildenafil

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

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b.a. Sweetie & Dave’s Chocolate Malt Ball Recall [US]

US FlagUS/Silver Spring: Logo - b.a. Sweetie Candy Co.b.a. Sweetie Candy Co., a Cleveland, Ohio establishment, recalls certain batch/lots of Chocolate Malt Balls and Chocolate Malted Milk Balls from the American marketplace due to undeclared Wheat, 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/a1YM30rDml7

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/ba-sweeties-candy-co-issues-voluntary-recall-its-chocolate-malt-chocolate-malted-milk-balls

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

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Antoto-K Thumbs Up 7 Red 70K Supplement Recall [US]

Antoto-K Thumbs Up 7 Red 70K Supplement Recall [US]

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US FlagUS/Silver Spring: Antoto-K, a Manassas, Virginia establishment, recalls all batch/lots of Thumbs Up 7 Red 70K Capsules from the American marketplace due to suspected 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/S1MB30rDgNO

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/antoto-k-issues-voluntary-nationwide-recall-thumbs-7-red-70k-due-presence-undeclared-sildenafil-and

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

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Harris Teeter & Dawn Food Cake Recall [US]

Harris Teeter & Dawn Food Cakes Recall [US]

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US FlagUS/Silver Spring: Rise Baking Company, a York, Pennsylvania establishment, recalls certain batch/lots of Harris Teeter branded Cookies and Creme Cakes as well as Dawn Food Products branded Vanilla Bean Waterfall Cakes from the American marketplace due to undeclared Hazelnuts, 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/YNcb30rD2On

Direct link: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/rise-baking-company-llc-issues-recall-undeclared-hazelnut-cakes

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

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