Faulty Drugs

FDA Recalls

April 30, 20246:21 pm
Gibson Farms Voluntarily Recalls Organic Light Halves and Pieces Shelled Walnuts Because of Possible Health... On 04/26/2024, Gibson Farms recalled Organic Light Halves and Pieces shelled walnuts because Gibson Farms received information that they may have the potential to be contaminated with E. Coli 0157:H7. E. coli O157:H7 causes a diarrheal illness often with bloody ...
April 27, 202410:23 pm
H-E-B Issues Voluntary Recall for 3-Ounce Cups of Creamy Creations Ice Cream in Select Flavors Committed to the safety and quality of its products, H-E-B is voluntarily issuing a recall for 12-count packages of 3-ounce cups of Creamy Creations ice cream in select flavors for potential metal. The affected products were distributed to all H-E-B ...
April 25, 20244:00 am
Tama Corporation Recalls Product Because of Possible Health Risk Tama Corporation of Doral FL is recalling 24-ounce containers of "Oueso de Mano PAISA" have contamination with Listeria monocytogenes, a bacterium that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened ...
April 23, 20245:02 pm
Dr. Reddy’s Issues Voluntary Nationwide Recall of Sapropterin Dihydrochloride Powder for Oral Solution 100 mg... Dr. Reddy's Laboratories Ltd. (BSE: 500124, NSE: DRREDDY, NYSE: RDY, NSEIFSC: DRREDDY, along with its subsidiaries together referred to as "Dr. Reddy's"), today announced that it is voluntarily recalling six (6) lots of Sapropterin Dihydrochloride Powder for Oral Solution 100 ...
April 22, 20243:30 pm
STOP CLOPEZ CORP Issues Voluntary Worldwide Recall of Schwinnng Capsules Due to the Presence of... Hollywood, FL, US, STOP CLOPEZ CORP is voluntarily recalling one lot of Schwinnng capsules to the consumer level. FDA analysis has found the Schwinnng products to contain Nortadalafil. Nortadalafil is an active drug ingredient known for the treatment of male ...
April 19, 20244:20 pm
Primal Kitchen Issues Voluntary Recall of Primal Kitchen Avocado Oil (750mL Glass) Due to Packaging... Primal Kitchen is announcing a voluntary recall of approximately 2,060 cases of three code dates of Primal Kitchen Avocado Oil (750mL) because the glass may be prone to breakage, causing the product to spill.
April 19, 20242:36 pm
Infinite Herbs, LLC Expands Recall of Fresh Organic Basil to Include Melissa’s Brand Organic Basil... Infinite Herbs LLC of Miami, Florida, is expanding its April 18th recall to include Melissa's brand fresh organic basil in 2.0 oz ( 96 packages, UPC 0 45255 14142 9) and 4.0 oz packages (24 packages, UPC 0 45255 14439 ...
April 19, 202412:24 am
Sammy’s Milk Providing a Warning Against the Use of Goat Milk Toddler Formula as Infant... Newport Beach, California - Sammy's Milk, a local company, has been asked by the Food and Drug Administration (FDA) to provide a warning against the use of its Goat Milk Toddler Formula as an infant formula because the FDA is ...
April 18, 20242:09 pm
Infinite Herbs, LLC Voluntarily Recalls 2.5-Ounce Fresh Organic Basil Sold From February 1 Through April... Infinite Herbs LLC of Miami, Florida, is voluntarily recalling 2.5-ounce packages of Infinite Herbs fresh organic basil sold between February 1 and April 6, 2024, and bearing the UPC 8 18042 02147 7 (see photos below) because they have the ...
April 13, 20246:00 pm
Cargill Conducts Voluntary Recall of Nutrena® Country Feeds® Meatbird 22% Crumble Due to Non-inclusion of... Cargill’s animal nutrition business is conducting a voluntary recall of Nutrena® Country Feeds® Meat bird 22% Crumble (RV) due to non-inclusion of Vitamin D. Lack of Vitamin D in meat bird diets can lead to mineral deficiencies and bone issues, ...
April 12, 20247:59 pm
Roly Poly Bakery Issues Allergy Alert on Undeclared Egg Ingredient in Multigrain Bread Roly Poly Bakery of New Britain, CT is recalling its 20 ounce loafs of Roly Poly multigrain bread because the product contains undeclared egg product. People who have allergies to eggs run the risk of serious or life-threatening allergic reaction ...
April 12, 20245:11 pm
Gracie’s Kitchen Inc. Issues Allergy Alert on Undeclared Sesame and Wheat Allergens in “Broccoli Cutlets” Gracie’s Kitchens of New Haven, CT, is recalling its 20-ounce packages of "King Kullen Broccoli Cutlets with Bread Crumbs and Parmesan" because they may contain undeclared sesame and wheat. People who have allergies to sesame and wheat run the risk ...
April 12, 20244:00 am
Feel Good Foods Issues Voluntary Recall of Gluten-Free Cream Cheese Stuffed Mini Bagels Feel Good Foods is voluntarily recalling its Gluten-Free Plain and Everything flavored Cream Cheese Stuffed Mini Bagels. The products may contain undeclared gluten that may be present due to cross-contamination. People who have an allergy or severe sensitivity to gluten ...
April 11, 202410:00 pm
ADM Animal Nutrition Expands Recall to Include 17 Additional Lots of Chicken, Swine and Rabbit... Specific lots may contain elevated levels of magnesium, sodium, calcium and/or phosphorus; may harm chickens, swine, rabbits.
April 10, 202411:24 pm
Oregon Spice Company Issues Allergy Alert on Undeclared Sesame in Johnny’s Parmesan Garlic Seasoning Oregon Spice Company, Portland, OR is recalling Johnny’s Parmesan Garlic Seasoning 5oz because it may contain undeclared sesame. People who have an allergy or severe sensitivity to sesame run the risk of serious or life-threatening allergic reaction if they consume ...
April 10, 20244:40 pm
Home Style Foods, Inc. Issues Allergy Alert on Undeclared Egg in Kowalski Simply Sides –... Home Style Foods, Inc., of Hamtramck, MI, is voluntarily recalling 43 cases of “Kowalski Simply Sides - Jack’s Potato Salad” due to an incorrect label resulting in an undeclared egg allergen. People who have an allergy or severe sensitivity ...
April 9, 20249:10 pm
Belgian Yummies Issues Allergy Alert on Undeclared Allergens of Wheat, Soy, Egg, Coconut and/or Peanuts... Belgian Yummies of Fort Myers, FL, is alerting the public that its 4-ounce packages of Ice Cream Sandwiches and 5-liter containers and 4.75-liter pans of Gelato contains undeclared allergens.
April 9, 20249:00 pm
Baron Spices, Inc. Issues Allergy Alert on Undeclared Soy and Wheat in Blues Hog Sweet... Baron Spices, Inc. of St. Louis, MO is recalling 708 units of Blues Hog Sweet and Savory Seasoning, because it may contain undeclared Soy and Wheat allergen. People who have an allergy or severe sensitivity to Soy and Wheat run ...
April 5, 20249:22 pm
Global Mix, Inc Recalls Tejocote Products Because of Possible Health Risk Global Mix, Inc. of New York, is recalling tejocote products to include the following brands: Eva Nutrition, Science of Alpha, Niwali, NWL Nutra. The recalled products are labeled as tejocote root but are toxic yellow oleander. Ingestion of yellow ...
April 5, 20247:30 pm
Medline Industries, LP Issues a Nationwide Recall of Convenience Kits Containing Nurse Assist 0.9% Sodium... Northfield, Ill., Apr. 5, 2024 – In direct response to the Nurse Assist, LLC voluntary product recall initiated on November 6, 2023, for saline and sterile water medical products, Medline Industries, LP initiated a nationwide recall on November 15, 2023, ...
February 6, 20246:22 pm
FDA adds Boxed Warning for increased risk of severe hypocalcemia in patients with advanced chronic... Listen to FDA Drug Safety Podcast titled, FDA adds Boxed Warning for increased risk of severe hypocalcemia in patients with advanced chronic kidney disease taking osteoporosis medicine Prolia (denosumab).
January 26, 20242:32 pm
Update on FDA’s ongoing evaluation of reports of suicidal thoughts or actions in patients taking... Listen to FDA Drug Safety Podcast, FDA's preliminary evaluation has not found evidence that use of GLP-1 RAs causes suicidal thoughts/actions.
December 8, 20232:07 pm
FDA warns of rare but serious drug reaction to the antiseizure medicines levetiracetam (Keppra, Keppra... Listen to an audio podcast of the November 28, 2023, FDA Drug Safety Communication, FDA warns of rare but serious drug reaction to the antiseizure medicines levetiracetam (Keppra, Keppra XR, Elepsia XR, Spritam) and clobazam (Onfi, Sympazan).
May 31, 20231:57 pm
FDA updating warnings to improve safe use of prescription stimulants used to treat ADHD and... Listen to an audio podcast of the May 11, 2023, FDA Drug Safety Communication on warnings to improve safe use of prescription stimulants used to treat ADHD and other conditions
May 10, 202310:43 am
FDA updates prescribing information for all opioid pain medicines to provide additional guidance for safe... Listen to an audio podcast of the April 13, 2023, FDA Drug Safety Communication, FDA updates prescribing information for all opioid pain medicines to provide additional guidance for safe use.
December 16, 20229:07 pm
FDA investigating risk of severe hypocalcemia in patients on dialysis receiving osteoporosis medicine Prolia (denosumab) FDA investigating risk of severe hypocalcemia in patients on dialysis receiving osteoporosis medicine Prolia (denosumab)
July 27, 20223:18 pm
FDA warns about possible increased risk of death and serious side effects with cancer drug... Listen to an audio podcast of the June 30, 2022, FDA Drug Safety Communication. Results from a clinical trial show a possible increased risk of death with Copiktra (active ingredient duvelisib) compared to another medicine to treat leukemia and lymphoma. ...
July 7, 20224:35 pm
FDA withdrew its approval for the cancer medicine Ukoniq (umbralisib) due to safety concerns Listen to an audio podcast of the 6/1/22 for Ukoniq . FDA withdrew its approval for the cancer medicine Ukoniq (active ingredient umbralisib) due to safety concerns. Ukoniq was approved to treat two specific types of lymphoma: marginal zone ...
April 13, 20224:17 pm
FDA recommends thyroid monitoring in babies and young children who receive injections of iodine-containing contrast... Listen to an audio podcast of the March 30, 2022 FDA Drug Safety Communication Iodinated Contrast Media
February 9, 20227:08 pm
FDA investigating possible increased risk of death with lymphoma medicine Ukoniq (umbralisib) Listen to an audio podcast of the February 3, 2022, FDA Drug Safety Communication, FDA is investigating a possible increased risk of death with the cancer medicine Ukoniq (umbralisib). We are re-evaluating this risk against the benefits of Ukoniq for ...

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