Alaska recalls

ANI Pharmaceuticals is recalling estradiol gel (0.1%, 0.25 mg packets) because some packets in affected cartons were found to be empty or only partially filled. This could mean patients receive less medication than prescribed. The recall affects carton lot M251109, which expires in November 2027.

Gas-X Simethicone 125 mg softgels distributed by Haleon are being recalled because the carton labeling does not list all inactive ingredients. This affects three specific lot codes (KB5Y, MP4B, and SS4F) distributed nationwide.

Lupin Pharmaceuticals is recalling certain batches of Liraglutide Injection (a diabetes and weight-loss medication) because white thread-like particles have been found inside the cartridges. The affected pens are distributed nationwide. No injuries have been reported.

Sagent Pharmaceuticals is recalling two lots of Busulfan Injection due to failed impurities and degradation specifications. The affected lots are 656412 (expiring 08/31/2026) and 659646 (expiring 03/31/2027). This is a prescription medication used in cancer treatment.

Amerisource Health Services has recalled certain batches of Primidone Tablets, USP, 50 mg due to cross-contamination during manufacturing. The tablets contain trace amounts of Acemetacin, a different active pharmaceutical ingredient, which should not be present in this medication.

Primidone tablets distributed by American Health Packaging were found to contain trace amounts of Acemetacin, a different active pharmaceutical ingredient, due to cross-contamination during manufacturing. The affected lot (1027583, expiring 09/30/2027) contains approximately 63,500 tablets distributed nationwide. No injuries have been reported.

Golden State Medical Supply's Primidone Tablets (250 mg) contain trace amounts of Acemetacin, a different medication, due to cross-contamination during manufacturing. This affects two lots distributed nationwide. No injuries have been reported.

Golden State Medical Supply is recalling Primidone 50 mg tablets because the active ingredient was contaminated with trace amounts of Acemetacin, a different medication. This contamination occurred during manufacturing. The affected bottles are identified by specific lot numbers with expiration dates in 2028.

Lannett Company's Primidone Tablets 250mg were contaminated during manufacturing with trace amounts of Acemetacin, a different active pharmaceutical ingredient. The contamination affected specific lot numbers distributed nationwide. No injuries have been reported.

Insulet found a manufacturing issue in certain lots of Omnipod 5, Omnipod DASH, and Omnipod Eros pods that could cause insulin to leak instead of being fully delivered into the body. The leak occurs when a small tear develops in the tubing just above the skin. In some cases, users may not notice the problem, which can lead to high blood sugar levels and, in severe cases, diabetic ketoacidosis.

Dexcom discovered that two lots of its G7 continuous glucose monitoring sensors—originally designated as scrap and scheduled for destruction—were stolen before being destroyed and sold by an unauthorized third party. One lot has an increased risk of skin infection due to improper sterilization; the other has an increased risk of sensor failure.

Mogo Moringa LLC is voluntarily recalling two specific lots of Mogo Moringa Oleifera Capsules due to a possible Salmonella contamination concern. The affected lots are Lot 15525AA (expires 06/2027) and Lot 00926AA (expires 01/2028). No Salmonella was detected in the company's own testing, but the recall is being issued as a precaution while the FDA continues its review.

JXK Enterprises is recalling Boner Bears Chocolate (Lot #BB21125) because FDA testing found sildenafil, the active ingredient in prescription Viagra, in the product—but it was not listed on the label. Sildenafil can cause serious interactions with certain heart and blood pressure medications and poses health risks for people with diabetes, high blood pressure, or heart disease.

The LED lights inside these decorative spheres can overheat and catch fire. The company has received nine reports of sparking or overheating, though no injuries have been reported so far.

These LED shot glasses contain button cell batteries in an easily accessible compartment. Children can remove and swallow the batteries, which can cause serious internal burns and death. The glasses also lack required safety warnings.

PandaEar portable hook-on chairs have a safety defect: the crotch restraints can be removed without tools, allowing infants to fall through an opening. This violates the mandatory safety standard for these products and poses a serious injury or death risk.

ORB Toys' Funkee squeeze toys may contain asbestos-like fibers in the sand filling. If the toy ruptures or leaks, inhaling this dust could cause serious health problems. The recalled toys have date code 3102491A and were sold at Walmart and Ollie's Bargain Outlet between February 2025 and April 2026.

HomeProGym-branded resistance bands can forcefully separate from the handle during use, creating a risk of serious impact injury. The recall affects only purple 60-pound and gray 70-pound bands sold in various sets and bundles between December 2025 and April 2026. No injuries have been reported so far.

ABC Trading toy headbands and electronic pet cages contain button cell batteries in compartments that children can easily open. Swallowing these batteries can cause serious internal burns and death.

Hometown Food Company recalled a single lot of Birch Benders 12 oz Sweet Potato Pancake and Waffle Mix because it may contain undeclared egg. The affected product has lot code 5265 and a best-if-used-by date of March 24, 2027. People with egg allergies or sensitivities could have a serious reaction if they consume it.

A software issue in the A810 Clinician Programmer App can cause infusion steps to display out of order in rare cases. When this happens, the SynchroMed Flex infusion pump may not deliver medication at the intended time, or not deliver it at all. The issue affects specific clinician tablet models running software versions 1.x and 2.x.

MicroVention LVIS stent-assist devices may have incorrect dimensions or configuration due to a manufacturing mix-up. Devices that are too large can damage blood vessel walls; devices that are too small may not expand properly or could cause blood clots and stroke.

Medtronic discovered that certain lots of the Marinr Steerable reprocessed electrophysiology catheter have incomplete seals on the sterile packaging. This affects 87 units distributed in the US, Canada, and Israel. No injuries have been reported.

Stryker Sustainability Solutions is recalling Daig Livewire Steerable BDB electrophysiology catheters (Product Number 401918) due to incomplete seals on the sterile packaging. This affects 2 units with specific lot numbers. Incomplete seals may allow contamination of the sterile product.

Stryker Sustainability Solutions issued a recall of Daig Livewire Steerable reprocessed electrophysiology catheters (Product Number 401932) due to incomplete seals on the sterile packaging. The incomplete seals could potentially allow contamination of the sterile product. A total of 458 units across multiple lot numbers were affected and distributed in the US, Canada, and Israel.

Stryker Sustainability Solutions identified incomplete seals on certain lots of the Daig Livewire Steerable reprocessed electrophysiology catheter (Product Number 401923). The affected units may not maintain sterility, which could pose a risk during use. Three units have been affected.

Stryker Sustainability Solutions identified incomplete seals on certain lots of Daig Livewire Steerable electrophysiology catheters. The incomplete seals may compromise sterility of the product. Approximately 206 units across multiple lot numbers were affected.

Stryker Sustainability Solutions recalled Daig Livewire Steerable electrophysiology catheters (Product Number 401914) due to incomplete seals on the sterile packaging. The defect affects 10 units across 10 lot numbers distributed in the US, Canada, and Israel. No injuries have been reported.

Stryker Sustainability Solutions is recalling Daig Livewire Steerable electrophysiology catheters (Product Number 401908) due to incomplete seals on the sterile packaging. This affects 3 units with specific lot numbers distributed in the US, Canada, and Israel. Incomplete seals could allow contamination of the sterile product.

Stryker Sustainability Solutions is recalling certain lots of the Daig Livewire Steerable electrophysiology catheter because some units have incomplete seals on their sterile packaging. This affects 107 catheters distributed in the U.S., Canada, and Israel. No injuries have been reported.