Tag: food_recalls

FDA Announces Class I Recall for BMC Luna G3 APAP Due to Firmware Flaw

8 Sep 2026 4:53 p.m. · Source: US Food and Drug Administration

BMC Medical's Luna G3 APAP devices face a Class I recall due to a firmware defect. The flaw can cause therapy failure, potentially leading to serious health consequences, with up to 196 units possibly still affected.

Health Business Science & Technology Medical Science Computers and Internet Legal Product Recall Medical Devices FDA BMC Medical Co., Ltd.Luna G3 APAP Firmware Defect Class I Recall Food Recalls Drugs
Fi Recalls Dog Supplements Over Salmonella Contamination Risk

8 Sep 2026 4:50 p.m. · Source: US Food and Drug Administration

Fi has issued a recall for its dog supplements due to potential Salmonella contamination from an ingredient. The recall affects animals and poses a risk to humans handling the product or animal waste. Customers are being notified.

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Made Fresh Salads Recalls Deli Products Over Listeria Contamination Risk

8 Sep 2026 4:49 p.m. · Source: US Food and Drug Administration

Made Fresh Salads Inc. is recalling all Ready to Eat Deli Style Salads and cream cheese due to potential Listeria monocytogenes contamination. Products were distributed in Brooklyn, Queens, Bronx, and New York City, with expiration dates through September 18, 2026.

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SUPPLX.com Recalls Male Enhancement Products Over Undeclared, Dangerous Yohimbine

8 Sep 2026 4:46 p.m. · Source: US Food and Drug Administration

SUPPLX.com recalls Business Pill and Branch Manager for Men due to undeclared, dangerously high yohimbine levels. This male enhancement ingredient can cause severe heart issues, gastrointestinal distress, and neurological effects, prompting a nationwide alert.

Health Business Medical Science Legal Social Issues SUPPLX.com Business Pill Branch Manager for Men Yohimbine Product Recall Dietary Supplements Male Sexual Enhancement Food Recalls FDA Drugs
Foods Alive Recalls Organic Moringa Leaf Powder Over Salmonella Risk

8 Sep 2026 4:43 p.m. · Source: US Food and Drug Administration

Foods Alive Inc. is recalling its 8-ounce organic moringa leaf powder nationwide due to potential *Salmonella* contamination. The FDA announced the recall, warning of serious health risks, though no illnesses have been reported yet.

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American Regent Recalls Epinephrine Injection Due to Particulate Matter and Sterility Issues

8 Sep 2026 4:42 p.m. · Source: US Food and Drug Administration

American Regent, Inc. is recalling three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) nationwide. The recall is prompted by leaking, cracked vials, and particulate matter, posing serious health risks and sterility concerns.

Health Business Medical Science Federal Government Legal Social Issues American Regent, Inc.Epinephrine Injection Product Recall Particulate Matter Sterility Pharmaceuticals FDA Food Recalls Drugs
SUPPLX.com Recalls Male Enhancement Products Over Undeclared, Dangerous Yohimbine Levels

6 Sep 2026 6:50 a.m. · Source: US Food and Drug Administration

SUPPLX.com recalls Business Pill and Branch Manager for Men due to undeclared, high levels of yohimbine. The substance, used for erectile dysfunction, poses serious health risks including hypertension, cardiac issues, and death, prompting an urgent consumer warning.

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Frozen Berry Blend Recalled Over E. coli O145 Contamination Risk

4 Sep 2026 12:34 p.m. · Source: US Food and Drug Administration

Frutas y Hortalizas del Sur S.A. expanded its recall of Great Value Organic Triple Berry Blend due to potential E. coli O145 contamination. Consumers should check freezers for lot 6040 01-6, discard or return it. No illnesses reported yet.

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B. Braun Medical Recalls Saline Injection Due to Particulate Matter Risk

4 Sep 2026 8:25 a.m. · Source: US Food and Drug Administration

B. Braun Medical is recalling three lots of 0.9% Sodium Chloride Injection USP nationwide due to particulate matter. This poses life-threatening risks like emboli and organ damage, though no adverse events have been reported yet.

Health Business Politics and Government Medical Science Federal Government Legal Social Issues B. Braun Medical Sodium Chloride Injection Product Recall Particulate Matter FDA Healthcare Pharmacy Food Recalls Drugs
American Regent Recalls Epinephrine Injection Over Particulate Matter and Sterility Risks

4 Sep 2026 8:14 a.m. · Source: US Food and Drug Administration

American Regent recalls three lots of Epinephrine Injection USP nationwide due to particulate matter and sterility concerns from cracked vials. This poses serious risks like blood clots and organ damage, though no adverse events have been reported yet.

Health Business Politics and Government Medical Science Federal Government Legal American Regent Epinephrine Injection Product Recall Particulate Matter Sterility Anaphylaxis FDA Food Recalls Drugs
FDA Issues Class I Recall for Boston Scientific Spinal Cord Stimulator Leads

3 Sep 2026 4:18 p.m. · Source: US Food and Drug Administration

The FDA has issued a Class I recall for Boston Scientific's unused Infinion CX Leads, part of Spinal Cord Stimulator Systems. Mechanical stress can cause lead fractures, leading to inadequate stimulation and 1,081 reported serious injuries. This recall affects only…

Health Business Politics and Government Medical Science Federal Government Legal Boston Scientific Infinion CX Leads Spinal Cord Stimulator FDA Product Recall Medical Devices Class I Recall Food Recalls Drugs
FDA Issues Early Alert for Draeger VentStar Resus Neo Hoses Due to Cracks

3 Sep 2026 4:11 p.m. · Source: US Food and Drug Administration

Draeger's VentStar Resus Neo hoses are subject to an FDA Early Alert due to reported cracks. This issue could lead to serious patient harm, including death, if used. No injuries or deaths have been reported as of August 27.

Health Business Science & Technology Medical Science Legal Federal Government Draeger VentStar Resus Neo Breathing Circuit Medical Device FDA Product Recall Patient Safety Food Recalls Drugs
FDA Classifies GE HealthCare Monitoring Software Issue as Class II Recall

3 Sep 2026 1:28 p.m. · Source: US Food and Drug Administration

The FDA has reclassified an early alert for GE HealthCare's Portrait Core Services Software as a Class II Recall. The issue, identified during a service update, has not led to patient monitoring disruptions.

Health Science & Technology Politics and Government Medical Science Computers and Internet Federal Government Legal GE HealthCare FDA Portrait Core Services Software Medical Device Product Recall Class II Recall Patient Monitoring Food Recalls Drugs
FDA Issues Early Alert for AVID Medical Kits Containing Recalled Sodium Chloride

2 Sep 2026 1:25 p.m. · Source: US Food and Drug Administration

AVID Medical convenience kits contain recalled sodium chloride ampules, raising sterility and quality concerns. The FDA issued an "Early Alert" due to potential risks of infection and severe complications, especially for critically ill patients and spinal procedures.

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B. Braun Medical Recalls Sodium Chloride Injection Over Iron Oxide Particles

1 Sep 2026 7:17 a.m. · Source: US Food and Drug Administration

B. Braun Medical is recalling three lots of 0.9% Sodium Chloride Injection USP nationwide due to iron oxide particulate matter. The FDA warns of life-threatening risks, including emboli and organ damage, though no adverse events have been reported.

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Ana Salazar Modela Tu Cuerpo Recalls Lipofit Extreme Fat Burner 2.0 Over Undeclared Fluoxetine and DNP

31 Aug 2026 4:35 p.m. · Source: US Food and Drug Administration

Ana Salazar Modela Tu Cuerpo Inc. has recalled Lipofit Extreme Fat Burner 2.0 nationwide. The weight-loss product contains undeclared fluoxetine and toxic DNP, posing serious health risks including cardiac arrest and neurological effects.

Health Business Politics and Government Medical Science Federal Government Legal Social Issues Product Recall Lipofit Extreme Fat Burner 2.0 Ana Salazar Modela Tu Cuerpo Inc.Fluoxetine 2,4-Dinitrophenol (DNP)Weight Loss US Food and Drug Administration Food Recalls FDA Drugs
Kofinas Olive Oil Recalls Garlic Infused Product Over Unapproved Ingredient

31 Aug 2026 4:34 p.m. · Source: US Food and Drug Administration

LMSI LLC/Kofinas Olive Oil voluntarily recalls its Garlic Mediterranean infused extra virgin olive oil. The recall is due to an unapproved garlic essential oil, affecting products sold in Cincinnati and online from August 2025 to August 2026.

Health Business Medical Science Legal Education Economy Product Recall LMSI LLC Kofinas Olive Oil Garlic Mediterranean infused extra virgin olive oil Cincinnati Food Safety Olive Oil Food Recalls FDA Drugs
Crystal Temptations Recalls Chocolatey Eyeballs Over Undeclared Milk

31 Aug 2026 4:28 p.m. · Source: US Food and Drug Administration

Crystal Temptations is recalling Halloween Chocolatey Eyeballs across 13 states due to undeclared milk allergens. Consumers with milk allergies face serious risks if they consume these products.

Health Business Medical Science Economy Education Product Recall Food Safety Allergy Alert Milk Allergy Crystal Temptations Chocolatey Eyeballs US Food and Drug Administration Food Recalls FDA Drugs
Panorama Produce Recalls Mangoes Over Salmonella Concerns

31 Aug 2026 4:26 p.m. · Source: US Food and Drug Administration

Panorama Produce is recalling 302 boxes of mangoes sold in CT, NY, NJ, and PA due to potential "Salmonella" contamination. No illnesses have been reported, but consumers should check for specific product identifiers.

Health Business Politics and Government Medical Science Legal Agriculture Federal Government Social Issues Panorama Produce Mangoes Salmonella Product Recall FDA Food Safety Northeast US Food Recalls Drugs
Everything Sprouts Expands Recall of Radish Mix Over E. Coli and Salmonella Concerns

31 Aug 2026 4:27 p.m. · Source: US Food and Drug Administration

Everything Sprouts, LLC has expanded its voluntary recall to include Robust Radish Sprout Mix due to potential contamination with E. coli and Salmonella. The product was distributed in Minnesota and Wisconsin, though no illnesses have been reported yet.

Health Business Medical Science Legal Education Social Issues Everything Sprouts Robust Radish Mix Product Recall E. coli Salmonella Food Safety Minnesota Wisconsin Food Recalls FDA Drugs
Northwest Naturals Recalls Raw Pet Food Over Salmonella and Listeria Concerns

31 Aug 2026 4:24 p.m. · Source: US Food and Drug Administration

Northwest Naturals has voluntarily recalled specific lots of its Frozen Chicken Recipe cat and dog food nationwide due to potential Salmonella and Listeria monocytogenes contamination, posing risks to pets and handlers. No illnesses have been reported.

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B. Braun Recalls Sodium Chloride Injection Over Particulate Matter Risk

28 Aug 2026 3:23 p.m. · Source: US Food and Drug Administration

B. Braun Medical Inc. has issued a nationwide recall for three lots of 0.9% Sodium Chloride Injection USP due to zinc oxide particulate matter. This recall addresses potential life-threatening health risks, including emboli and organ damage, though no adverse events…

Health Business Medical Science Legal Product Recall B. Braun Medical Inc.Sodium Chloride Injection Particulate Matter Zinc Oxide FDA Food Recalls Drugs
Baxter Recalls Saline Solution Over Fiberglass Contamination Risk

28 Aug 2026 3:21 p.m. · Source: US Food and Drug Administration

Baxter International has issued a nationwide recall for two lots of 0.9% Sodium Chloride Injection due to potential fiberglass particulate matter. This contamination poses serious health risks, including blood clots and organ damage, though no adverse events have been reported…

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FDA Issues Early Alert for Avid Medical IV Start Kit Recall Over Fungal Contamination

28 Aug 2026 2:10 p.m. · Source: US Food and Drug Administration

Avid Medical is recalling IV Start Kits due to fungal contamination risk from included BD ChloraPrep applicators. The FDA issued an Early Alert, warning of serious health consequences like infection and sepsis, though no injuries or deaths have been reported.

Health Business Medical Science Legal Education Social Issues Avid Medical IV Start Kit Product Recall FDA Aspergillus penicillioides BD ChloraPrep Medical Devices Food Recalls Drugs
Boston Scientific Recalls Angiographic Catheters Over Tip Detachment Risk

28 Aug 2026 1:58 p.m. · Source: US Food and Drug Administration

The FDA has issued an Early Alert for Boston Scientific's Imager II Angiographic Catheters, which are being recalled due to a manufacturing defect risking tip detachment. Two serious injuries have been reported, prompting the company to discontinue the product.

Health Business Politics and Government Medical Science Federal Government Legal Boston Scientific Imager II Angiographic Catheters FDA Medical Device Recall Tip Detachment Embolism Early Alert Food Recalls Drugs
B. Braun Medical Recalls Sodium Chloride Injection Over Particulate Matter Risk

28 Aug 2026 12:56 p.m. · Source: US Food and Drug Administration

B. Braun Medical has issued a nationwide recall for three lots of 0.9% Sodium Chloride Injection USP due to zinc oxide particulate matter, which could lead to life-threatening health consequences, though no adverse events have been reported.

Health Business Medical Science Federal Government Legal Social Issues B. Braun Medical Sodium Chloride Injection Product Recall Particulate Matter Zinc Oxide FDA Healthcare Food Recalls Drugs
AVID Medical Issues Class I Recall for Kits with Contaminated Medline Manifolds

27 Aug 2026 12:22 p.m. · Source: US Food and Drug Administration

AVID Medical has issued a Class I recall for convenience kits containing Medline Namic Star Off Handle Manifolds due to particulate contamination. The FDA warns of serious injury or death if these components are not removed, though no incidents have…

Health Business Medical Science Federal Government Legal AVID Medical Medline Namic Star Off Handle Manifolds Class I Recall FDA Product Recall Medical Devices Food Recalls Drugs
Medtronic Issues Early Alert for Bravo CF Capsule Delivery Devices Over Serious Injury Risks

27 Aug 2026 11:20 a.m. · Source: US Food and Drug Administration

Medtronic and Given Imaging issued an Early Alert for Bravo CF capsule delivery devices, citing risks of attachment/detachment failure. This issue has led to 184 serious injuries, prompting a recommendation for device removal due to deployment control problems.

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Revival Animal Health Recalls Feline Milk Replacers Over Nutrient Deficiencies

26 Aug 2026 4:04 p.m. · Source: US Food and Drug Administration

Revival Animal Health has recalled Breeder’s Edge® and Shelter’s Choice® Feline Milk Replacers nationwide due to inconsistent vitamin and mineral levels. These deficiencies pose severe, potentially fatal health risks to vulnerable kittens, prompting an urgent warning to consumers.

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Jaime’s Foods ATX Recalls Jalapeno Ranch Over Undeclared Egg Allergen

26 Aug 2026 4:02 p.m. · Source: US Food and Drug Administration

Jaime’s Foods ATX is recalling its Jalapeno Ranch dressing due to undeclared egg, a serious allergen risk. Sold in Texas Central Market and Austin independent stores from April 3, 2026, the recall affects 16 oz jars with specific lot numbers.…

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