Wisconsin recalls

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.

The LinkBio CORE Workstation, part of the CORE Shoulder System, may show an incorrect Planning Date when you view cases in the Start Case menu. This could lead to confusion about case timing. Five units are affected across Alabama, Florida, and Kansas.

Certain versions of the iLet Ace Pump software (1.3.7, 1.4.2, and 1.4.3) have a security flaw that allows someone to bypass the Lock Screen and Limited Access Passcode Screen by pressing icons in the status bar. This could let an unauthorized person make false meal announcements or stop insulin delivery, risking severe low blood sugar.

Remel's Yeastone Broth (11ML, 10/BOX, model YY3462) may give wrong results when labs use it to test how fungi respond to antifungal medicines. If a lab doesn't catch the bad result during its own quality checks, doctors might delay treatment or switch to a different antifungal drug unnecessarily.

Philips AneurysmFlow is software used by doctors to help evaluate aneurysm treatment with flow diverter stents. The software's Mean Aneurysm Flow Amplitude (MAFA) ratio does not reliably predict whether the aneurysm is successfully closed, but doctors may be using it to make treatment decisions based on the user manual.

B Braun Medical Inc is recalling specific hemodialysis bloodline tubing (Model B3-4630M4705) because small air bubbles can accumulate in the arterial line when blood gases stick to the tubing under negative pressure. This could affect dialysis treatment safety. The recall affects units manufactured since August 5, 2025.

B. Braun Medical Inc is recalling specific hemodialysis bloodline tubing because small air bubbles can accumulate in the arterial line during dialysis treatment. This happens when blood gases stick to the tubing when negative pressure is applied. The affected units were manufactured on or after August 1, 2025.

B. Braun Medical Inc is recalling certain hemodialysis bloodlines (model SL-2000M2095L) because small air bubbles can collect in the arterial line when the tubing is under negative pressure. This happens because blood gases stick to the inside of the tubing. No injuries have been reported.

Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.

Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.

B. Braun Medical Inc is recalling STREAMLINE BLOODLINE SET FOR DIALOG DR. (Model SL-2010M2096A) due to a potential risk of small air bubbles accumulating in the arterial line during hemodialysis treatment. This happens when blood gases stick to the tubing under negative pressure, which could affect treatment safety. The recall affects units manufactured on or after June 9, 2025.

Certain Omnipod 5 Pods from 49 specific manufacturing lots contain an internal tear in the soft cannula. This defect causes insulin to leak inside the Pod instead of being delivered to your body. In some cases, the Pod may shut down completely and stop delivering insulin, or deliver less insulin than needed.

Avantor Performance Materials has recalled Magnesium Chloride, 6-Hydrate Crystal (500G bottles, Lot 23G3161005, expiration 9/21/2027) because the product does not meet strength specifications. This bulk pharmaceutical ingredient may be less potent than labeled.

Island Kinetics, Inc. (d.b.a. CoValence Laboratories) is recalling specific lots of Skin Script Blemish Spot Treatment because the product failed stability testing. This means the product may not maintain its intended strength or safety over time. No injuries have been reported.

Major Pharmaceuticals is recalling memantine hydrochloride extended-release 7 mg capsules (lot N02425, expiring 05/31/2027) because the capsules may not dissolve properly in the body. This means the medication may not work as intended. The affected capsules were distributed nationwide.