B&I Overseas Trading Recalls Product Due to Potential Contamination with Listeria Monocytogenes

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B&I Overseas Trading Inc from Van Nuys, CA is recalling frozen “Veladis herring in oil with Italian spices” because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, a

Source: Food and Drugs Administration--Recalls/Safety Alerts

Shane Erickson, Inc. DBA Innovative Marketing Consultants Issues Voluntary Nationwide Recall of Wash-Free Hand Sanitizer Due to Potential Presence of Undeclared Methanol

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Shane Erickson, Inc. is voluntarily recalling lot 2020/05/11 and MFG: 2020/05/10 L/N: 20200510-3 of imc Wash-Free Hand Sanitizer 50 ml, 100 ml, 300 ml and Wash Free Hand Sanitizer 300 ml lot 2020/05/11 and Thrifty White Pharmacy Wash-Free Hand Sanitizer 300 ml lot 2020/05/11 listed in the table belo

Source: Food and Drugs Administration--Recalls/Safety Alerts

B&G Foods Issues Voluntary Allergy Alert on Undeclared Soy in a Limited Number of Containers of Food Club Garlic Powder That Incorrectly Contain Bacon-Flavored Bits

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B&G Foods announced today it is voluntarily recalling individual containers of 5.37 oz. Food Club Garlic Powder, with “best by” dates of NOV 19 22 and NOV 20 22, because they mistakenly contain bacon-flavored bits, which contain soy, an allergen undeclared on the garlic powder labels. People who ha

Source: Food and Drugs Administration--Recalls/Safety Alerts

Country Fresh Announces Voluntary Limited Recall of SE Grocers Branded Party Tray with Vegetables and Ranch Dip Due to Undeclared Allergens

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Country Fresh Orlando, FL., is recalling a limited number of cases of product containing a vegetable tray with ranch dip due to a possible health risk from an undeclared allergen in a product.

Source: FDA Food Safety Recalls RSS Feed

Country Fresh Announces Voluntary Limited Recall of SE Grocers Branded Party Tray with Vegetables and Ranch Dip Due to Undeclared Allergens

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Country Fresh Orlando, FL., is recalling a limited number of cases of product containing a vegetable tray with ranch dip due to a possible health risk from an undeclared allergen in a product.

Source: Food and Drugs Administration--Recalls/Safety Alerts

O&H Danish Bakery, Inc. Issues Allergy Alert on Potential for Undeclared Pecans in Almond Kringle

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O&H Danish Bakery, Inc. of Racine, WI is recalling 3,173 units of Almond Kringle (1lb 8oz) with batch code 26720 sold in Trader Joe’s retail stores because it may contain undeclared Pecans. People who have allergies to pecans run the risk of serious or life-threatening allergic reaction if they cons

Source: FDA Food Safety Recalls RSS Feed

Tesoros Trading Company Recalls Product Because of Possible Health Risk

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Tesoros Trading Co. from Las Vegas, NV is recalling certain codes of frozen “Trader Joe’s Lightly Salted Edamame” because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly peo

Source: Food and Drugs Administration--Recalls/Safety Alerts

Torrent Pharmaceuticals Limited Issues Voluntary Nationwide Recall of Anagrelide Capsules, USP Due to Dissolution Test Failure

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Torrent Pharmaceuticals Limited is voluntarily recalling one lot of Anagrelide Capsules, USP to the consumer level due to dissolution test failure detected during routine quality testing.

Source: Food and Drugs Administration--Recalls/Safety Alerts

Torrent Pharmaceuticals Limited Issues Voluntary Nationwide Recall of Anagrelide Capsules, USP Due to Dissolution Test Failure

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Torrent Pharmaceuticals Limited is voluntarily recalling one lot of Anagrelide Capsules, USP to the consumer level due to dissolution test failure detected during routine quality testing.

Source: Food and Drugs Administration--Recalls/Safety Alerts

AvKARE Issues Voluntary Nationwide Recall of Sildenafil 100mg Tablets and Trazodone 100mg Tablets Due to Product Mix-Up

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AvKARE, Pulaski, TN is voluntarily recalling one lot of Sildenafil 100 mg tablets and one lot of Trazodone 100mg tablets to the consumer level. These products have been recalled due to a product mix-up of the listed two separate products inadvertently packaged together during bottling at a 3rd party

Source: Food and Drugs Administration--Recalls/Safety Alerts