Alaska recalls

GE HealthCare identified a potential electrical cable issue on certain Allia Moveo angiographic X-ray systems equipped with Gaia generators. Service personnel who work inside the equipment cabinet while power is on could be exposed to electrical shock during installation, maintenance, or troubleshooting.

GE HealthCare identified a potential electrical cable issue on certain Allia IGS Pulse angiographic X-ray systems equipped with Gaia generators. Service personnel performing installation, maintenance, or troubleshooting work inside the C-FRT cabinet while power is on could be exposed to electrical shock.

GE HealthCare identified a faulty electrical cable on certain Allia IGS 7 Pulse angiographic X-ray systems equipped with Gaia generators. Service personnel working inside the C-FRT cabinet while the system is powered on could receive an electrical shock during installation, maintenance, or troubleshooting.

GE HealthCare identified a potential electrical cable issue on certain Allia IGS 5 Pulse angiographic X-ray systems equipped with Gaia generators. Service personnel performing installation, maintenance, or troubleshooting inside the C-FRT cabinet while power is on face a risk of electrical shock.

GE HealthCare identified a potential electrical cable issue on certain Allia IGS 3 Pulse angiographic X-ray systems equipped with Gaia generators. Service personnel performing installation, maintenance, or troubleshooting work inside the C-FRT cabinet while the system is powered on could be at risk of electrical shock.

The Plum Duo Precision IV Pump may fail to display a soft limit alert under certain conditions, meaning clinicians won't be notified before the pump starts delivering medication that exceeds the set safety limit. This could result in patients receiving too much or too little medication.

The Plum Duo Infusion Pump may fail to display alerts when medication delivery limits are exceeded. Without these warnings, clinicians may not know before the pump starts delivering the wrong amount of medication to a patient.

The Plum Solo Precision IV Pump may fail to display a soft limit alert under certain conditions, preventing clinicians from being notified of dosage limit violations before the pump starts delivery. This could result in incorrect medication doses being administered.

A manufacturing defect in the Fresh Roast Systems ColorTrack model BENCH R-100 could, under rare misuse conditions, expose users to infrared laser light levels higher than the product's safety rating. No injuries have been reported. The defect affects a small number of units.

U.S. Trading Company is recalling DRAGONFLY Thai Ginger Powder (4.37 oz) because it may contain lead. The powder was distributed across multiple U.S. states. No injuries have been reported.

Total Nutrition Inc is recalling TNVitamins and Doctor's Pride brand moringa capsule supplements because they may be contaminated with Salmonella. The recall affects 13,000 bottles sold nationwide across multiple lot numbers.

Park St. Deli Macaroni & Cheese (20 oz packages) contains soy lecithin that is not listed on the label. People with a soy allergy or sensitivity could have a serious reaction if they eat this product without knowing soy is present.

Refresqueria Estrella Inc. is recalling Bebida de Parcha (passion fruit drink) in multiple sizes because the product contains FD&C Red 40 food coloring that was not declared on the label. This affects bottles sold in Puerto Rico with specific production lot codes and expiration dates from March through May.

Sun Pharmaceutical has recalled budesonide inhalation suspension (1mg/2mL single-dose ampules) due to the presence of black or brown specs and particles found in some vials. The affected lot is BAG0074A with an expiration date of January 31, 2027. This is a quality issue that could affect the safety and sterility of the medication.

Ascend Laboratories is recalling Minocycline Hydrochloride Extended-Release Tablets, 115 mg (lot 25141635, expires 4/30/2028) because testing found the tablets did not dissolve properly as required. This affects 360 bottles distributed nationwide. No injuries have been reported.

Gas-X Extra Strength softgels were contaminated with a diluted propylene glycol-based coolant during packaging due to a machine leak. The contamination affected specific lot numbers distributed nationwide. No injuries have been reported.

Golden State Medical Supply is recalling specific lots of niacin extended-release tablets (1,000 mg) because they failed to dissolve properly during stability testing. The tablets did not meet dissolution specifications at the 24-hour mark, which means they may not release the medication as intended in the body.

Zep Inc. is recalling Alcohol Sanitizer Spray (Ethanol 70%, 55-gallon drums) due to microbial contamination. The affected batch (E2612116, expiration April 2029) was distributed nationwide. A total of 5 drums are involved.

Amneal Pharmaceuticals is recalling Primidone 50 mg tablets (NDC 53746-544-01, lot AM251676) due to potential cross-contamination with Acemetacin during manufacturing at the API supplier. The contamination could affect the safety or effectiveness of the medication.

Breckenridge Pharmaceutical is recalling specific lots of Duloxetine Delayed-Release Capsules 60mg due to higher-than-acceptable levels of a chemical impurity called N-nitroso-duloxetine. This impurity was found during manufacturing quality checks. The recall affects about 360,000 bottles distributed nationwide.

Breckenridge Pharmaceutical is recalling one lot of Duloxetine Delayed-Release Capsules 30mg due to the presence of N-nitroso-duloxetine impurity above FDA's recommended interim limit. This is a manufacturing quality issue. No injuries have been reported.

Fresenius Kabi USA is recalling specific batches of epinephrine injection due to failed impurity and degradation specifications. The affected vials may not meet required purity standards. No injuries have been reported.

Sun Pharmaceutical's doxorubicin hydrochloride liposome injection vials were found to contain glass particles. The affected vials are lot HAG2581B, which expire in May 2027. About 675 vials were distributed nationwide.

Beekeeper's Naturals Saline Nasal Spray was manufactured without proper sterilization, allowing microbial contamination. The affected product is Lot #5950 with an expiration date of 02/2028. No injuries have been reported so far.

Sensory Supplement LLC is recalling Neuro Nourish dietary supplement due to premature lipid oxidation that can cause an off odor and bitter taste. The affected product is a 5.9 oz multi-nutrient supplement sold online nationwide. No injuries have been reported.

Nara Organics is recalling all lots of its powdered infant formula due to potential contamination with Clostridium botulinum, a bacteria that can cause infant botulism. Three infants who consumed the formula were hospitalized with botulism in California, Washington, and Pennsylvania, though none died. The formula was sold at Target and Nara.com between July 2025 and June 2026.

Beekeeper's Naturals is recalling one lot of its Saline Nasal Spray sold on Amazon because it contains elevated levels of yeast and may be contaminated with Aspergillus, a fungus that can cause serious infections in people with weakened immune systems or lung disease. The company has received four reports of sinus congestion, irritation, or infection potentially linked to this product.

Kidisle single-serve coffeemakers can become clogged, causing hot liquid or steam to build up and spray out unexpectedly during use. The CPSC has received at least 107 reports of this happening, with 27 injuries including first and second-degree burns requiring medical care.

Yamaha UMAX Bistro and Bistro Deluxe vehicles (Model Years 2019–2025) have an incorrect weight capacity label. If the label is wrong, the vehicle could be overloaded, creating a risk of injury to operators or bystanders.

These white plastic drain covers do not meet federal safety standards required by the Virginia Graeme Baker Pool and Spa Safety Act. They lack required safety markings, warnings about service life, and installation instructions, creating a risk of entrapment and drowning.