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Author: Asebey Law

29 September
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Albertsons Companies Voluntarily Recalls Select Store-Made Deli Items Containing Bowtie Pasta Supplied by Fresh Creative Foods Due to an Ingredient Recall for Possible Listeria monocytogenes Contamination

Posted by Asebey Law
in FDA News

Following a recall initiated by Fresh Creative Foods, a division of Reser’s Fine Foods, Inc., Albertsons Companies has voluntarily recalled five store-made deli items, supplied by Fresh Creative Foods, due to possible Listeria monocytogenes contamination. The recall was initiated because these produ Read More (external link)...

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26 September
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SLR Food Distribution, Inc. Recalls Wise Wife Brand Ground Cinnamon Because of Possible Health Risk

Posted by Asebey Law
in FDA News

SLR Food Distribution of Hicksville, NY is recalling Wise Wife brand Cinnamon, because it has the potential to be contaminated with elevated levels of lead. Short term exposures to very low levels of lead may not elicit any symptoms. It is possible that increased blood lead levels may be the only Read More (external link)...

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26 September
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Georgia Nut Company (GNC), Third-Party Manufacturer for Tru Fru, LLC Issues Voluntary Recall of Specific Varieties of Tru Fru Freeze Dried Products Due to Potential Presence of Metal in Product

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in FDA News

Today, Tru Fru, LLC announced that its third-party manufacturer, Georgia Nut Company (GNC) issued a voluntary recall of specific varieties of Tru Fru Freeze Dried products due to the potential presence of metal in the product. Hard or sharp foreign objects in food may cause traumatic injury includi Read More (external link)...

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26 September
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Gansu Zhaofeng Agricultural Development Co., Ltd. Is Voluntarily Recalling Its Dried Bean Curd Due to Undeclared Wheat

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in FDA News

Gansu Zhaofeng Agricultural Development Co., Ltd.in Hui County Industrial Concentration Zone, Longnan City, Gansu Province has voluntarily recalled 500g/bag G&L FOOD Dried Bean Curd for failing to declare the allergen wheat. People who have an allergy or severe sensitivity to wheat run the risk of s Read More (external link)...

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23 September
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Lawrence Wholesale LLC Recalls Kroger Bagged Frozen Shrimp and Kroger Frozen Shrimp Products Because of Possible Health Risk

Posted by Asebey Law
in FDA News

Lawrence Wholesale LLC of Vernon, CA is recalling a limited quantity of Kroger bagged frozen shrimp and Kroger frozen shrimp products because they may have been prepared, packed, or held under insanitary conditions whereby they may have become contaminated with Cesium-137 (Cs-137). Read More (external link)...

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23 September
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Updated Release: Southwind Foods, LLC Recalls Frozen Shrimp Because of Possible Health Risk

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in FDA News

Southwind Foods, LLC of Carson, California is voluntarily recalling a limited quantity of Frozen Shrimp, due to possible radionuclide (Cesium-137) contamination. Cs-137 is a manmade radioisotope of cesium. Traces of Cs-137 are widespread and can be present in the environment at background levels, an Read More (external link)...

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20 September
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Western United Fish Company Recalls Kirkland Signature Brand Ahi Tuna Wasabi Poke Because of Possible Health Risk

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in FDA News

September 20, 2025, Western United Fish Company dba Annasea Foods Group of Kent, WA is recalling 3,314.7 lbs. of Kirkland Signature brand Ahi Tuna Wasabi Poke, Costco Item Number of 17193, with the Sell By Date of 9/22/2025, because the green onions used in the product have the potential to be cont Read More (external link)...

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20 September
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Aquastar (USA) Corp Recalls Kroger Frozen Raw EZ Peel, Kroger Mercado Frozen Cooked Shrimp, and Aquastar Raw Shrimp Skewers Because of Possible Health Risk

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in FDA News

September 19, 2025, AquaStar (USA) Corp of Seattle, WA is recalling: approximately 49,920 bags (net wt. 2lbs) of Kroger Raw Colossal EZ Peel Shrimp approximately 18,000 bags (net wt. 2lbs) of Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp approximately 17,264 bags (net wt. 1.25lbs) of AquaSt Read More (external link)...

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19 September
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Olympus Issues Voluntary Recall for Specific Lots of ViziShot 2 FLEX (19G) EBUS -TBNA Needles

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in FDA News

CENTER VALLEY, Pa., (September 19, 2025) — Olympus Corporation has announced a voluntary, global medical device removal action for ViziShot 2 FLEX (19G) EBUS -TBNA needles (“ViziShot 2 FLEX”) manufactured prior to May 12, 2025, after receiving reports of device components detaching during procedures Read More (external link)...

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Asebey Life Science Law is a boutique law firm specializing in FDA regulatory compliance, transactional law, and advisory services for the life sciences industry.

501 E Las Olas Blvd. | Suite 300
Fort Lauderdale, FL 33301

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