Arizona recalls

Blackwing Organic Meats sold beef and pork products that were produced without required federal inspection and some bear false USDA inspection marks. These products may contain harmful bacteria, allergens, or other contaminants. The affected products were produced between April 2024 and March 2026 and shipped nationwide.

Great Value Small Curd Cottage Cheese (16oz, 24oz, and 3lb sizes) may be under-pasteurized due to a broken seal on the pasteurizer. The products were distributed to Walmart stores in 11 states. No illnesses have been reported.

Great Value Lowfat Cottage Cheese Small Curd (24 oz, UPC 0 78742 11673 0) may be under-pasteurized due to a broken seal on the pasteurizer. The affected products have "Best If Used By" dates of April 1–3, 2026 (lot #06-71) and were distributed to 11 states.

Saputo Cheese USA is recalling Great Value Fat Free Cottage Cheese (24 oz tubs) because a broken seal on the pasteurizer may have allowed the product to be under-pasteurized. Under-pasteurized dairy products can contain harmful bacteria. The affected products were distributed to Walmart stores in 11 states.

Potentially under pasteurized. The firm was notified by the California Department of Agriculture that due to the broken seal on the pasteurizer, the products may be under pasteurized, and they should recall the products.

Clover Sonoma low-fat cottage cheese may not have been fully pasteurized due to a broken seal on processing equipment. The affected products were distributed to 11 states. No illnesses have been reported.

MID EAST Jordanian Zaatar spice mix in 5 lb bags contains sesame and wheat that are not listed on the label. This product was distributed to bakeries for use in breads and pastries. People with sesame or wheat allergies could have a serious reaction if they consume products made with this spice mix.

Winder Laboratories is recalling certain batches of their grape-flavored multivitamin with fluoride chewable tablets because they contain less vitamin D than stated on the label. The FDA discovered this during an inspection. The affected products are the 0.25 mg and 1 mg formulations with specific lot numbers and expiration dates in October and November 2025.

Apotex Corp. is recalling specific lots of brimonidine tartrate/timolol maleate eye drops because the manufacturer cannot confirm the product was sterilized properly. The affected lots are VJ8599 (expires 09/30/2026) and VL1668 (expires 01/31/2027). No infections or injuries have been reported so far.

Somerset Therapeutics is recalling one lot of dexamethasone sodium phosphate injection because testing found impurity levels above acceptable limits as the product approached its expiration date. The affected lot (A240421, expiring 07/31/2026) was distributed nationwide. No injuries have been reported.

Strides Pharma Children's Ibuprofen Oral Suspension (100 mg per 5 mL) has been recalled because some bottles contain gel-like masses and black particles. The affected bottles are 4 FL OZ (120 mL) size with lot numbers 7261973A or 7261974A, expiring 01/31/2027. No injuries have been reported.

Shaman Botanicals is recalling White Vein Advanced Alkaloids chewable tablets because testing found the active ingredient (7-hydroxymitragynine) is present in higher amounts than stated on the label. The label says 7.5 mg per serving, but the actual content is greater. No injuries have been reported.

One lot of Amneal Magnesium Sulfate in Water for Injection IV bags was found to contain the wrong medication—Tranexamic Acid—inside the packaging. This mix-up affects hospitals that received the product between late December 2025 and late February 2026. No patients have been harmed so far.

Aisstxoer brand adult bicycle helmets sold on Amazon do not meet safety standards for impact protection and fit stability. If you crash while wearing one, the helmet may fail to protect your head, risking serious injury or death.

The blade on Amazon Basics Camping Folding Pocket Knives can fail to stay closed, creating a risk of cuts. Amazon received one report of the blade opening unexpectedly, though no injuries have been reported so far.

Certain Frigidaire gas ranges can have a delayed ignition in the oven's bake burner, which may cause a sudden flame burst and burn injuries. About 174,800 ranges are affected, sold between June 2025 and January 2026. Electrolux Group and the CPSC have received 62 reports of delayed ignition and 30 reports of burn injuries.

Goregent-branded infant walkers sold on Amazon can fit through standard doorways and do not stop at the edge of stairs, creating a serious fall risk. About 90 walkers with model number 901 and a yellow production label dated November 2025 are affected. No injuries have been reported yet.

BUILT brand LUUM light up tumblers can crack or break, exposing the button cell battery inside. Children can access and swallow these small batteries, which can cause serious internal burns, chemical injuries, or death. One child has already put a battery from one of these tumblers in their mouth.

Specialized electric bicycles in the Como SL line have forks that can develop small cracks over time, which may lead to fork failure and cause the rider to fall. The company has received one report of a fork failure but no injuries so far.

Tainoki Fine Furniture is recalling height-adjustable swivel office chairs sold at HomeGoods because the metal base can bend during use, creating a fall risk. The recall affects Noah, Owen, and Warren model chairs sold between August and December 2025. No injuries have been reported.

Wagner power steamers can develop an excessively hot hose and may expel hot water during or after use, even after you release the trigger. The company has received over 50 reports of burn injuries, including first- and second-degree burns to arms, hands, feet, and faces.

Medline surgical drapes and gowns may fall apart (delaminate) when washed using the included instructions. If a delaminated drape is used during surgery, it could tear and allow bacteria through, increasing infection risk.

Medline surgical gowns may develop fabric separation (delamination) when laundered using the included instructions. If a separated gown is used during surgery, fluid or bacteria could pass through the compromised fabric, potentially increasing infection risk.

Medline and Cardinal Health have recalled specific lots of chest drainage kits used in cardiac surgery because the instructions needed to clarify that these devices are intended only for adult patients age 18 and older. The kits were distributed nationwide in California and internationally to Chile and Panama.

Altruan GmbH distributed Bisaf Strep A Self-Test kits without FDA clearance. This test is designed to detect group A streptococcal antigens in throat swabs, but has not been reviewed or approved by the FDA for safety and effectiveness. About 188 units were distributed nationwide.

Altruan GmbH distributed Clearest Strep-A Cassette Test kits that were not cleared or approved by the FDA before being sold. These tests are designed to detect group A streptococci (Strep A) in throat swab samples. About 188 units were distributed nationwide.

Wondfo Streptococcal A At-Home Self-Test kits were distributed in the US without FDA clearance. This means the test's accuracy and safety have not been verified by the FDA. If you have this test, results may not be reliable.

The Lutronic CLARITY II Laser System (Model 1110200210) may spark or pop during use, potentially causing burns to patients. The FDA has identified over 1,500 affected units based on serial number.

The Covidien HealthCast Vital Sync remote patient monitoring system has a defect that can prevent critical patient alarms from being transmitted from bedside monitors to remote monitoring stations. This means clinicians may not receive timely alerts about patient condition changes. The FDA has identified 78 affected systems.

International Life Sciences is recalling Artelon FLEXBAND TWIST surgical augmentation devices (lot RK29976) because they failed bacterial endotoxin testing. Bacterial endotoxins are substances that can trigger harmful immune responses if present on medical devices used in surgery.