IKEA Expands Recall of Mirrors Due to Laceration Hazard

The plastic fittings that attach the mirror to the wall can break, causing the mirror to fall, posing a laceration hazard to consumers.

Source: Recall List

SugarMDs LLC Issues Voluntary Nationwide Recall of Advanced Glucose Support Supplements Capsules Due to Presence of Undeclared Glyburide and Metformin

Maryland Heights, MO, SugarMDs, LLC is voluntarily recalling Lot: 22165-003 Advance Glucose Support Supplement in 60, 120 and 180 count bottles to the consumer level. FDA analysis has found the product to be tainted with glyburide and metformin. Glyburide and Metformin are active ingredients found

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

SugarMDs LLC Issues Voluntary Nationwide Recall of Advanced Glucose Support Supplements Capsules Due to Presence of Undeclared Glyburide and Metformin

Maryland Heights, MO, SugarMDs, LLC is voluntarily recalling Lot: 22165-003 Advance Glucose Support Supplement in 60, 120 and 180 count bottles to the consumer level. FDA analysis has found the product to be tainted with glyburide and metformin. Glyburide and Metformin are active ingredients found

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

Sofia Produce, LLC DBA Trufresh Recalls Fresh Cantaloupe Because of Possible Health Risk Due to Salmonella

SOFIA PRODUCE, LLC, of Nogales, Arizona which does business under the name “Trufresh” (“Trufresh”) is recalling all sizes of fresh cantaloupes packaged in cardboard containers labeled with the “Malichita” label, sold under the following sales order numbers between October 16, 2023 and October 23, 20

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

Sofia Produce, LLC DBA Trufresh Recalls Fresh Cantaloupe Because of Possible Health Risk Due to Salmonella

SOFIA PRODUCE, LLC, of Nogales, Arizona which does business under the name “Trufresh” (“Trufresh”) is recalling all sizes of fresh cantaloupes packaged in cardboard containers labeled with the “Malichita” label, sold under the following sales order numbers between October 16, 2023 and October 23, 20

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

Botanical-Be Issues Voluntary Nationwide Recall of Kuka Flex Forte, Reumo Flex (Caplets) and Artri King (Tablets). Due to Presence of Undeclared Diclofenac

November 7, 2023 – In El Paso, TX, Botanical-Be has voluntarily initiated a recall of all batches of Kuka Flex Forte caplets, Reumo Flex caplets, and Artri King tablets. This recall is directed at the consumer

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

Nurse Assist, LLC Issues Recall of 0.9% Sodium Chloride Irrigation USP and Sterile Water for Irrigation USP Nationwide and to Canada

Nurse Assist, LLC initiated a voluntary recall of 0.9% sodium chloride irrigation USP and sterile water for irrigation USP, due to the potential for a lack of sterility assurance, which could result in a nonsterile product. In populations most at risk, such as patients who are immunocompromised, the

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

Nurse Assist, LLC Issues Recall of 0.9% Sodium Chloride Irrigation USP and Sterile Water for Irrigation USP Nationwide and to Canada

Nurse Assist, LLC initiated a voluntary recall of 0.9% sodium chloride irrigation USP and sterile water for irrigation USP, due to the potential for a lack of sterility assurance, which could result in a nonsterile product. In populations most at risk, such as patients who are immunocompromised, the

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

Grandy Organics Issues Allergy Alert on Undeclared Coconut in Gluten Free Honey Oat Granola

Grandy Organics of Hiram, Maine is voluntarily recalling Gluten Free Honey Oat Granola with lot code 231017-03459-1 because it may contain undeclared Coconut. People who have an allergy or severe sensitivity to coconut run the risk of serious or life-threatening allergic reaction should they consume

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

Grizzly Lathe Defect Can Cause Serious Injuries

Grizzly Industrial has recalled two brands of wood lathes because the cutting tool may break and become a projectile and injure the user or anyone nearby.

Grizzly issued the recall on Nov. 2, 2023, for 21,300 Grizzly Industrial and Shop Fox wood lathes, according to an announcement with the U.S. Consumer Product Safety Commission.

  Grizzly lathe defect can cause serious injuries   Injuries resulting from defective products can result in substantial physical, emotional, and financial stress. If you or someone you know has been injured by a faulty or defective product, the attorneys at our office may be able to help. Contact our product liability attorneys today, Call (214) 390-4173 or submit your case.  

Source: Recall List