Louisiana recalls

Raw Farm has recalled specific batches of raw cheddar cheese products (blocks and shredded) due to a potential link to an E. coli O157:H7 outbreak. The recall includes multiple batch numbers and expiration dates listed on the Raw Farm website. No pathogens have been found in Raw Farm products tested so far.

The canopy beams on certain Samson International bed frames can collapse, especially when the bed is moved. The company has received five reports of the canopy collapsing and striking people, resulting in shoulder and head injuries.

Tuymec Minoxidil Hair Growth Spray bottles sold on Amazon do not have child-resistant caps, violating federal safety rules. Minoxidil is toxic if swallowed by young children and can cause serious injury or death.

Sam's Club is recalling Member's Mark Valentine-themed children's pajama sets because they don't meet mandatory flammability standards for sleepwear. This poses a risk of burn injuries. About 18,000 sets were sold online between December 2025 and January 2026.

HTRC and Haisito brand T400 battery chargers can overheat and ignite, causing fires or explosions. The company has received 33 reports of fires and explosions, including three reports of injuries from burns and smoke inhalation.

Sangohe portable bed rails (models 504E and 504Q) can trap users between the rail and mattress, creating a serious risk of injury or death by asphyxiation. The rails also lack required warning labels. About 36,500 units were sold online starting August 2023.

The metal cap on the handle screw of these sauté pans can detach and eject forcefully when the pan is heated. E Mishan has received at least 98 reports of the cap detaching, including one case where a consumer was bruised and burned.

TecFlox minoxidil topical solution bottles do not have child-resistant packaging as required by law. The liquid inside can cause serious injury or death if a young child swallows it. About 900 bottles were sold on Amazon in October 2025.

ELENKER portable bed rails can trap users between the rail and mattress, creating a serious risk of injury or death by asphyxiation. The rails also lack required warning labels. The recalled models are silver collapsible rails sold on Amazon since August 2023.

OCUN NA is recalling certain Condor HMS Triple Carabiners sold from February 2025 through February 2026. The carabiner's gate can fail to close automatically and may require manual closing, which could cause the carabiner to fail during climbing and lead to a fall.

These Christmas light-up party favors contain button cell batteries that children can easily access and swallow. Swallowed button batteries can cause serious internal burns and death. The rings were sold on Amazon between August and December 2025.

These Halloween light-up rings contain easily accessible button cell batteries that children can remove and swallow. Swallowed button batteries can cause serious internal burns and death within hours. About 800 units were sold on Amazon between June 2025 and January 2026.

Beestech spiral tower toys sold on Amazon contain small plastic balls and are marketed for children under 3 years old, violating federal toy safety rules. The small balls pose a serious choking hazard. About 200 units were sold between November and December 2025.

The surgical instruction guide for the Waldemar Link Embrace Drill Tower shoulder instrument contains mixed-up article numbers in the equipment overview section. The individual surgical steps themselves are correct and safe to follow.

Waldemar Link's Embrace Shoulder Instruments Drill Tower (25mm, Item 645-081/62) was distributed with a surgical technique guide that lists incorrect article numbers in the instrument overview. The step-by-step surgical instructions themselves are correct and safe to follow.

Medline Industries has recalled specific lots of Puracol and Puracol Plus collagen wound dressings due to elevated endotoxin levels. These contaminants can cause inflammation, tissue irritation, delayed healing, fever, low blood pressure, and in severe cases, septic shock.

The labeling on BD Alaris System with Guardrails Suite MX does not specify which version of Transport Layer Security (TLS) must be enabled on hospital networks for secure Wi-Fi communication with Point-of-Care Units. This could create confusion during setup and potentially leave devices with inadequate security settings.

Olympus discovered that some PKS Cutting Forceps (Model 920005PK) have defective welds in their components. During surgery, the forceps' jaw can break due to these weak welds, potentially affecting the procedure.

Olympus PKS Cutting Forceps (Model 920000PK) contain welding defects that can cause the instrument's jaw to break during surgery. The supplier did not properly validate the welding process on affected components. This affects 7 units distributed worldwide.

Olympus Corporation has recalled its PKS Cutting Forceps (Model 3005PK) used during minimally invasive surgery. The device contains components with defective welds that were not properly validated by the supplier. If the jaw breaks during use, it could affect the procedure and patient safety.

Olympus discovered that some HALO PKS Cutting Forceps (model HACF0533) have defective welds in their components. During surgery, the forceps' jaw can break when the welds fail, potentially affecting the procedure. This affects medical facilities worldwide that use these surgical instruments with the Gyrus ACMI G400 Workstation.

Olympus PK Cutting Forceps (model PK-CF0533) contain welding defects that can cause the instrument's jaw to break during surgical use. The supplier did not properly validate the welding process on affected components. This could compromise the forceps' function during endoscopic or open surgical procedures.

Olympus discovered that some Everest Bipolar Cutting Forceps (Model 3006) have welding defects in internal components. These defects can cause the forceps' jaw to break during surgery, potentially requiring additional procedures or intervention.

Olympus has recalled its Everest Bipolar Cutting Forceps (Model 3005) used in minimally invasive surgery because some units contain defective welds in their components. The jaw of the forceps can break during use due to these faulty welds. This affects 106 units distributed worldwide.

Tandem Diabetes Care insulin pumps distributed in the Czech Republic and Slovakia have translation errors in their Czech language user guide. The most serious error tells users to verify the infusion set is connected to the body when it should say the opposite—that it should NOT be connected. Following these incorrect instructions could cause unintended insulin delivery and dangerously low blood sugar.

Medtronic has recalled certain MiniMed 780G insulin pumps due to software defects that can cause the pump to deliver too much insulin, too little insulin, or stop delivering insulin entirely. These defects appeared after software updates (versions 6.60, 6.61, and 6.62) and may result in dangerously high or low blood sugar levels. The recall affects over 26,000 pumps with specific serial numbers.

AMO has recalled certain TECNIS Eyhance intraocular lenses (IOLs) used in cataract surgery because a small number may have a defect where the lens haptic (support arm) sticks to the optic, preventing proper unfolding during implantation. This affects 361 lenses distributed across 12 U.S. states. No injuries have been reported.

A material mix-up had occurred during the manufacturing of Straumann¿ Custom Abutments. More specifically, a raw material bar of TAN-material (SAP #701924 / Lot 7130439) was incorrectly identified as a Titanium Bar Ti Gr4 D (SAP #701922 / Lot 7130430). As a result, RC Titanium abutments were manufactured using the TAN Bar material on Mill-from-Bar Machine 396-06.

Straumann USA LLC recalled certain Custom Abutment Ti units (catalog number 027.4620) because of a manufacturing error. A raw material bar made of TAN material was mistakenly labeled and used instead of the correct Titanium Grade 4 material during production. This affects 13 units distributed in the US and Canada.

Koven Technology's BiDop 3 Pocket Doppler ultrasound device was distributed with labeling that claims it can be used for fetal applications, but the FDA never approved it for that use. The device is only cleared to detect blood flow in blood vessels, not for fetal monitoring. Using it for unapproved purposes could lead to incorrect results or missed diagnoses.