Alabama recalls

Elekta has recalled certain Leksell Gamma Knife Perfexion and Icon radiosurgery systems because an adapter component may not be properly aligned or locked in place. This could affect the accuracy of radiation delivery during treatment. No injuries have been reported.

Some Stryker Cub Pediatric Cribs sold in the USA are missing two warning labels on the access doors. This affects 590 cribs with specific serial numbers. No injuries have been reported.

LeMaitre Vascular is recalling one unit of Artegraft Vascular Graft (Model AG740) distributed in Illinois due to a labeling mix-up on the outer packaging. The product box was labeled with an incorrect lot number, which could cause confusion during clinical use. No injuries have been reported.

The Welch Allyn Spot Vision Screener VS100 (software version 3.2.0.1) may display an unintended flickering screen due to a software issue. Flickering lights can trigger seizures in people who are photosensitive.

The external screws that secure the cover on the Howmedica Osteonics MICS3 Angled Sagittal Saw Attachment may loosen during use and detach. This affects all units with part number 210490 distributed across the United States and several other countries. No injuries have been reported.

GE Medical Systems' Centricity Universal Viewer software versions 5.0 SP6 through 5.0 SP7.1 has a cybersecurity weakness that may expose user login credentials on affected workstations. An unauthorized person could potentially use these exposed credentials to access the system, disrupt service, or alter medical images and data.

Certain versions of GE Centricity Universal Viewer software (versions 6.0 through 6.0 Sp10.4.1) contain a cybersecurity vulnerability that may expose user login credentials on affected workstations. An unauthorized person could potentially access the system and interfere with medical imaging data or system availability.

Certain versions of GE Centricity Universal Viewer software (versions 7.0 through 7.0 Sp2.0.1) contain a cybersecurity vulnerability that may expose user login credentials on workstations. An unauthorized person could potentially access the system and disrupt service or alter medical image data.

Abbott Diagnostics has recalled certain lots of the ID NOW Influenza A & B 2 test kit because they produce an unusually high number of invalid results compared to what the instructions say to expect. Invalid results mean the test does not give a clear positive or negative answer, requiring a retest.

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.