News wire

Recalls and safety alerts

Drug, device, food, vehicle and consumer product recalls and safety communications.

Checked 7 min ago · 31 of 35 sources responding · Sources and method

Filter stories (1)
Mass torts and MDLsProduct liabilityRecalls and safety alertsMedical malpracticeTrucking and commercial vehiclesMotor vehicle crashesAviationPremises liabilitySexual abuseWrongful deathVerdicts and settlementsClass actionsInsurance and bad faithLegislation and tort reformCourts and rulesAttorney disciplineLegal ethicsLegal technology and AIBar and practice news

Recalls and safety alerts

Recall U.S. Food and Drug Administration (Recalls)

A&P Creations LLC Issues Nationwide Recall of biQ-FEL Due to Undeclared Sildenafil and Tadalafil

Sildenafil and Tadalafil are active ingredients in FDA-approved prescription drugs Viagra and Cialis, respectively, used to treat erectile dysfunction. FDA approval of Viagra and Cialis is restricted to use under the supervision of a licensed health care professional. These undeclared ingredients ma

AgencyU.S. Food and Drug AdministrationRecalls and safety alerts

Read at U.S. Food and Drug Administration (Recalls)

Recall U.S. Food and Drug Administration (Recalls)

Wakefern Food Corp. Voluntarily Recalls Wholesome Pantry Organic Unsweetened Apple Sauce

KEASBEY, N.J. (Sept. 14, 2026) –Wakefern Food Corp. has voluntarily recalled select containers of Wholesome Pantry Organic Unsweetened Apple Sauce after routine FDA testing identified elevated patulin levels that exceed food safety limits and do not meet Wakefern's quality standards

AgencyU.S. Food and Drug AdministrationRecalls and safety alerts

Read at U.S. Food and Drug Administration (Recalls)

Safety notice U.S. Food and Drug Administration (Recalls)

Whole Foods Market Issues Allergy Alert on Undeclared Egg in Cabricharme Cheese

Whole Foods Market of Austin, TX is recalling Fromagerie Coop de Mean Cabricharme cheese because the product contains egg lysozyme, an egg white protein, which is not declared on the product label. People who have an allergy or severe sensitivity to eggs run the risk of a serious or life-threateni

Recalls and safety alerts

Read at U.S. Food and Drug Administration (Recalls)

Recall U.S. Food and Drug Administration (Recalls)

Centric Compounding Issues Nationwide Recall of Glutathione, Myer’s Cocktail, and Tri-Immune Boost Due to Elevated Endotoxin Levels

FOR IMMEDIATE RELEASE – 9/9/2026 – Houston, Texas, Centric Compounding is voluntarily recalling 6 lots of Glutathione 200mg/mL, Myer’s Cocktail, and Tri-Immune Boost injectable vials to the consumer level. The products have been found to be compounded with a Glutathione API containing elevated endot

Recalls and safety alerts

Read at U.S. Food and Drug Administration (Recalls)

Recall U.S. Food and Drug Administration (Recalls)

Evergreen Fresh Sprouts LLC Recalls Broccoli Sprouts Because of Possible Health Risk

09/10/2026, Evergreen Fresh Sprouts LLC of Moyie Springs, IDAHO is recalling 215 cases (6/4oz bags per case) of Broccoli Sprouts, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly pe

Recalls and safety alerts

Read at U.S. Food and Drug Administration (Recalls)

Recall U.S. Consumer Product Safety Commission (Recalls)

Victgoal Recalls Bicycle Helmets Due to Risk of Serious Injury or Death from Head Injury; Violate Mandatory Standard for Bicycle Helmets

The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the retention system, positional stability and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.

Recalls and safety alerts

Read at U.S. Consumer Product Safety Commission (Recalls)

Recall U.S. Consumer Product Safety Commission (Recalls)

Junkins Recalls DHASUWT Hair Dryer Brushes Due to Risk of Serious Injury or Death from Electrocution, and Shock Hazards; Violate Federal Regulations; Smoking and Fire Hazards

The recalled hair dryer brushes lack an integrated immersion protection device, which presents a substantial product hazard to consumers, posing the risk of death or serious injury from electrocution or shock if the hair dryers fall into water while plugged in to an electrical source. The recalled hair dryer brushes also pose the risk of death or serious injury from smoking and fire hazards.

Recalls and safety alerts

Read at U.S. Consumer Product Safety Commission (Recalls)

Recall U.S. Food and Drug Administration (Recalls)

FreshPoint Issues Recall Due to an Improperly Declared Allergen (Egg) in Chicken Salad Wedge Sandwiches

September 4, 2026 Orlando, FL– FreshPoint of Orlando, FL., is issuing a voluntary recall of 1,093 units of specific lots of Cranberry Chicken Salad Wedge sandwiches due to an improperly declared allergen (eggs). People who have an allergy or severe sensitivity to eggs run the risk of serious or lif

Recalls and safety alerts

Read at U.S. Food and Drug Administration (Recalls)

Recall U.S. Food and Drug Administration (MedWatch)

BMC Medical Co., Ltd. Recalls Luna G3 APAP (Model LG3600) with Firmware G3-2.00.76 Due to Firmware Defect

On July 15, 2026, BMC Medical Co., Ltd. (BMC), Beijing, China, retrospectively reported to the US Food and Drug Administration (FDA) a recall of 20,160 Luna G3 APAP (Model LG3600) devices distributed in the United States due to firmware defect. This corrective action was not reported to customers. O

AgencyU.S. Food and Drug AdministrationRecalls and safety alerts

Read at U.S. Food and Drug Administration (MedWatch)

Recall U.S. Food and Drug Administration (MedWatch)

B. Braun Medical Inc. Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container Due to the Presence of Particulate Matter

FOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container, to the hospital/healthcare facility/user level due to presence of particulate matter identified

Recalls and safety alerts

Read at U.S. Food and Drug Administration (MedWatch)