Wisconsin recalls

Furnulem 5-drawer dressers can tip over and trap children if not anchored to a wall. The dressers do not meet federal safety standards for clothing storage units. About 50 dressers were sold online in July 2025.

Kitosun Submersible LED Lights contain coin batteries (CR2450 and CR2032) that children can easily access and swallow. These batteries can cause serious internal burns and death if ingested. The lights lack required safety warnings.

Gumili Wintergreen Essential Oil sold on Amazon does not have child-resistant packaging, even though federal law requires it for products containing methyl salicylate. Young children who swallow the oil could be seriously poisoned.

Organic Zing Birch Essential Oil bottles sold on Amazon do not have child-resistant caps as required by law. The oil contains methyl salicylate, which can cause serious poisoning if a young child swallows it. About 940 bottles were sold between January 2024 and November 2025.

Little Cow Company's 9 oz soy candles in glass jars can crack or break during normal use, creating a risk of fire, burns, and cuts from broken glass. Two jars have broken so far, though no injuries have been reported yet.

Lola Plus The Boys has recalled five styles of youth hoodies and clothing sets with drawstrings that can get caught on objects and pose a strangulation risk to children. The drawstrings do not meet federal safety standards for children's upper outerwear. About 620 items were sold between November 2022 and September 2025.

Semfri children's helmets sold online do not meet mandatory safety standards for bicycle helmets. They may fail to protect a child's head in a crash, creating a serious risk of injury. About 300 medium-sized helmets in various colors were sold through Walmart.com between June and November 2025.

Shintenchi 6-drawer dressers can tip over if not bolted to the wall, creating a serious risk of injury or death to children. The white wooden dressers with golden metal feet (model SHX12077-WH) do not meet federal safety standards for furniture stability.

Lotus Joy Organic Sweet Birch Essential Oil bottles do not have child-resistant caps, even though the product contains methyl salicylate—a toxic substance if swallowed. Young children can easily open these bottles and drink the contents, which can cause serious poisoning or death.

Miach Orthopaedics BEAR Implant Model 1000 units have an incorrect expiration date printed on the label that extends beyond the product's actual shelf life. Because the expiration date is wrong, the UDI (Unique Device Identifier) is also incorrect. This affects 284 units distributed nationwide.

LSL Healthcare's Central Line Dressing Kit (Model 2519CP) contains BD ChloraPrep Triple Swabsticks with damaged packaging—some applicator seals are open. An open seal can allow the sterile applicator to become contaminated before use. This affects about 1,400 kits distributed in Idaho with lot number 5G3119 and expiration date 7/31/26.

LimFlow Vector vascular devices (Model VT-US-23, Lot 82321838) were distributed with an incorrect expiration date printed on the packaging. This affects 33 units distributed across multiple U.S. states. An incorrect expiration date could lead to use of a device beyond its safe lifespan.

Some BD Alaris Pump Module 8100 infusion pumps have a software date/time issue related to daylight saving time that may prevent them from connecting to hospital networks. This affects only the network connectivity function; the pump's ability to deliver medication is not impacted. The issue involves 189 devices distributed in Arizona, Indiana, Ohio, and Virginia.

Philips SmartPath to dStream MR imaging systems with software versions R11.1 and R12.1 may display incorrect stiffness values when MR Elastography maps are exported to a PACS viewer. This could affect the accuracy of tissue stiffness measurements used for clinical assessment. Three units have been identified worldwide.

Philips dStream 3.0T MRI systems with software versions R11.1 and R12.1 may display incorrect stiffness values when elastography images are sent to picture archiving systems (PACS). This affects the accuracy of tissue stiffness measurements used in clinical diagnosis.

Philips MR 7700 MRI systems running software versions R11.1 or R12.1 may display incorrect stiffness values when MR Elastography images are exported to a PACS viewer. This could affect the accuracy of tissue stiffness measurements used in clinical evaluation.

Philips MR 7700 MRI systems with software versions R11.1 and R12.1 may display incorrect stiffness values when elastography maps are exported to medical imaging viewing systems. This affects 9 units worldwide. No injuries have been reported.

Philips Ingenia Elition X MRI systems with certain software versions (R11.1 and R12.1) may display incorrect stiffness values when MR elastography maps are exported to a PACS viewer. This could lead to misinterpretation of tissue stiffness measurements used in clinical diagnosis.

Philips Ingenia Elition S MRI systems with software versions R11.1 and R12.1 may display incorrect stiffness values when MR Elastography maps are exported to a PACS (Picture Archiving and Communication System). This could affect the accuracy of tissue stiffness measurements used in clinical evaluation. Five units worldwide have been identified.

Philips has identified a potential error in how stiffness values are displayed when MR Elastography (MRE) images are exported to a PACS viewer on certain Ingenia Ambition X MRI systems. This affects 21 systems worldwide running software versions R11.1 or R12.1. The error could result in incorrect stiffness measurements being shown to clinicians.

Philips has recalled certain Ingenia Ambition S. MRI systems (software versions R11.1 and R12.1) because they may display incorrect stiffness values when MR Elastography images are sent to a PACS (picture viewing system). This could affect the accuracy of medical imaging data used for diagnosis.

Philips has recalled certain Ingenia 3.0T CX MRI systems (software versions R11.1 and R12.1) because stiffness values displayed in exported elastography maps may be inaccurate when viewed in a PACS (Picture Archiving and Communication System). This affects 6 units worldwide, primarily in the United States and Europe.

Philips has identified a software issue in certain Ingenia 3.0T MRI systems that may cause incorrect stiffness values to appear when viewing elastography images on a PACS (picture viewing system). This affects 24 systems worldwide with specific software versions. No injuries have been reported.

Philips has recalled certain Ingenia 1.5T MRI systems with software versions R11.1 and R12.1. When MR Elastography stiffness maps are exported to a PACS viewer, the stiffness values may display incorrectly. This could affect the accuracy of diagnostic information viewed in those systems.

Philips MR systems (Evolution Upgrade 3.0T, software versions R11.1 and R12.1) may display incorrect stiffness values when MR Elastography maps are exported to a PACS viewer system. This could affect the accuracy of imaging data used in clinical assessment.

Philips Evolution Upgrade 1.5T MRI systems with software versions R11.1 and R12.1 may display incorrect stiffness values when elastography maps are exported to a PACS viewer. This could affect the accuracy of tissue stiffness measurements used in clinical diagnosis. Three units have been identified worldwide.

Cardinal Health is updating instructions for multiple chest drainage unit models to clarify they are intended only for adults 18 years and older. When used on infants, these devices may not show proper bubbling or fluid movement, which can make it hard for clinicians to tell if the device is working correctly. This could delay or prevent needed treatment.

The touchscreen on certain Zimmer A.T.S. 3200TS tourniquet systems may freeze or stop responding when the device is set to operate in certain non-English languages. This could delay surgery while staff locate an alternate device. The issue affects systems running software version 2.06 or earlier.

The screen on Zimmer A.T.S. 5000TS Tourniquet Systems may freeze or stop responding when used in certain non-English language settings. This can delay surgery while staff locate an alternate device. The issue affects systems running software version v2.04 or earlier.

Medline medical procedure convenience kits containing MASTISOL liquid adhesive were recalled because the tubing can crack when the adhesive vial is opened. This could prevent proper use of the adhesive during surgery. No injuries have been reported.