Oklahoma recalls

Alliance Chemical's 1-K Kerosene Heater Fuel containers lack required safety features: flame mitigation devices to prevent flash fires and child-resistant closures to prevent accidental burns or poisoning. These containers violate federal portable fuel container safety standards.

Thermos food jars and bottles with certain model numbers can build up pressure when storing food or drinks for extended periods. When opened, the stopper may forcefully pop out and strike the user's face or eyes, causing serious cuts and injuries. Thermos has received 27 injury reports, including three cases of permanent vision loss.

Teva Pharmaceuticals is recalling specific lots of Claravis (isotretinoin) 10 mg capsules because they contain higher-than-allowed levels of tretinoin, a related chemical impurity. The affected lots are 100067507 and 100067508, which expire on July 31, 2026. No injuries have been reported so far.

B. Braun Medical is recalling two lots of Lactated Ringer's Injection (1L, product code E7500) because the solution contains unwanted particles, including cellulose and stearates. If these particles enter a patient's bloodstream during use, they could cause serious complications including blood clots, tissue damage, or organ failure.

Ghirardelli Chocolate Company is recalling certain powdered beverage mixes because they may be contaminated with Salmonella. The contamination came from a milk powder ingredient supplied by California Dairies, Inc. No illnesses have been reported so far.

The fence handles on this toy barn set can detach and pose a serious choking risk to young children. The toy is marketed for children under 3 years old but contains small parts that violate federal safety rules. About 3,000 sets sold on Amazon between July 2023 and June 2025.

CetoPMax baby loungers sold on Amazon fail to meet safety standards because the foam padding can block an infant's airway, creating a serious suffocation risk. About 2,100 loungers were sold between October and November 2025.

HappyGira baby loungers have sides that are too short, lack a stand, and have a sleeping pad that is too thick. Infants can fall out or become trapped, creating a serious suffocation and fall hazard. About 70 loungers sold online between September 2025 and February 2026 are affected.

BlissfulDestiny magnetic stick figure toys contain loose magnets that can separate and be swallowed by children. When multiple high-powered magnets are ingested, they can attract each other inside the digestive system, causing serious internal injuries including perforations, blockages, and blood poisoning.

32 Degrees heated socks can overheat and cause burns when worn during high-intensity activities that combine heat, friction, moisture, and pressure. The socks were sold at Costco from August 2025 through March 2026. Fourteen heat-related incidents have been reported, including burns.

Autobrush Sonic Pro Kids toothbrush delivery boxes contain a coin cell battery that children can easily access and swallow. Swallowing these batteries can cause serious internal burns or death. The packaging also lacks required warning labels.

AMZCMJ DGD-branded wooden kitchen tower stools can collapse or tip over during use. Children can also become trapped through openings on the sides of the stool. The company has received seven reports of children falling or becoming entrapped, with four resulting in injuries including contusions, splinters, and scrapes.

TOETOL HOME tower stools (model DETD0001) can collapse or tip over during use, and children can become trapped through openings in the sides. The company has received 18 reports of collapses resulting in injuries including cuts, scrapes, and contusions.

Weight plates can unexpectedly come loose from Tzumi FitRx SmartBell adjustable dumbbells during use, creating a serious falling-weight hazard. More than 115 cases of plates dislodging have been reported, resulting in at least six injuries including broken toes and cuts. The recall affects model 8361 dumbbells (5–52.5 lbs) sold at Walmart from January through November 2024.

Wiifo brand children's tower stools can collapse or tip over during use. A child's torso can also fit through openings on the sides, creating a risk of entrapment. The company has received 22 reports of stools collapsing, with 6 resulting in injuries including bruises and scrapes.

mGanna Sodium Hydroxide pellet bags sold on Amazon do not have child-resistant packaging, as required by law. The product is a caustic chemical that can cause serious chemical burns and eye damage if a child accesses it. About 3,240 bags were sold between November 2024 and March 2026.

Philips has identified three software issues in the Spectral CT on Rails Model 728334 that may affect scan operations. The gantry (rotating scanner) may not move to the correct position after pressing start; a required confirmation message may not appear; and a menu option may become unavailable during brain imaging setup. Three systems worldwide are affected.

Medline distributed one lot of CENTURION Circumcision Kits (lot number 25KLA002) without completing the required sterilization process. This means the kits are not sterile and could pose an infection risk if used. The affected kits were distributed in South Carolina.

The Gentuity HF-OCT Imaging System may display repeated image frames during a pullback procedure when used with certain catheters, which could affect the accuracy of length measurements. This issue affects specific software versions (21.11 to 23.3.13) paired with Vis-Rx and Vis-Rx Prime catheters. No injuries have been reported.

The centrifuge bowl on certain Cellex Photopheresis System kits may be difficult to install properly onto its holder. If not installed correctly, the bowl can break during use, which could delay patient treatment and cause blood loss.

Clariance-SAS is recalling multiple lots of Elegance Anterior Cervical Plates (used in neck spine surgery) due to burrs found on some finished plates. The burrs are sharp edges that could cause injury during or after implantation. No injuries have been reported so far.

Integra LifeSciences' Cytal Burn Matrix 10x15 cm (Product ID: BMM1015) has been recalled because certain lots tested at higher-than-acceptable endotoxin levels. Endotoxins are bacterial substances that can trigger inflammatory reactions when in contact with body tissues. The FDA identified this issue across 226 units distributed nationwide.

Integra LifeSciences has recalled specific lots of Cytal Burn Matrix (a burn wound dressing) because testing found higher-than-acceptable levels of endotoxin, a bacterial substance that can trigger an immune response. Seven units were distributed across the U.S. No injuries have been reported.

Increased rate of out-of-specification endotoxin results.

Integra LifeSciences' Cytal Wound Matrix 2-Layer (7x10 cm) from specific lot numbers tested higher than safe endotoxin levels. Endotoxins are bacterial substances that can trigger harmful immune responses. No injuries have been reported so far.

Integra LifeSciences' Cytal Wound Matrix 2-Layer 5x5 cm wound dressing (Product ID: WSM0505) has been recalled because some units have higher-than-safe levels of endotoxin, a bacterial substance that can trigger immune reactions. The affected product was distributed nationwide, and no injuries have been reported so far.

3B Medical distributed 2 units of the React Health PHOENIX 5L Oxygen Concentrator that did not meet the company's internal quality standards. The devices were distributed in New York. No injuries have been reported.

Siemens has recalled certain ARTIS Pheno VE30A and VE40A imaging systems used in hospitals and medical facilities. During 3D imaging procedures, these systems may produce images with uneven brightness, potentially leading to less accurate reconstructions and unintended low-dose radiation exposure to patients.

Wilson-Cook Medical is recalling Instinct Plus Endoscopic Clipping Devices (model G58010) due to increased complaints about potential device malfunction during use. The recall affects units manufactured between September 2, 2023 and April 20, 2025 and distributed worldwide. No injuries have been reported.

Certain Arjo Tenor mobile patient lifts contain actuators with an internal component that may not be strong enough to safely hold the load. In the worst case, this could cause the lifting arm to suddenly drop uncontrolled. This affects 119 units with specific serial numbers manufactured in certain batches.