Kentucky recalls

Waldemar Link GmbH & Co. KG is recalling a specific lot of Endo-Model Replacement Plateau knee implant screws (Item 15-2835/12, Lot 241210/1809). The bushing on the screw can potentially detach from the shaft due to a crack, which could affect the stability of the implant.

Waldemar Link GmbH & Co. KG is recalling specific lots of the Endo-Model SL Connection Component with PE-Plateau (Item 16-2840/07) used in orthopedic implants. The bushing on the plateau screw could detach from the screw shaft due to a longitudinal fracture, which could affect implant stability. Thirty-one units have been distributed outside the US.

Waldemar Link GmbH & Co. KG is recalling specific lots of Endo-Model SL Connection Component implant screws. The bushing on the plateau screw could detach from the screw shaft due to a crack, which could affect implant stability.

Waldemar Link GmbH & Co. KG is recalling Endo-Model Replacement Plateau screws (Item Number 15-0027/15) because the bushing could detach from the screw shaft due to a crack. This could affect the stability of the implant. Three units with lot number 2549190 were distributed worldwide, including in the U.S., Canada, and Europe.

Waldemar Link GmbH & Co. KG is recalling specific lots of the Endo-Model SL Connection Component (Item 16-2840/05) used in orthopedic implants. A bushing on the plateau screw could detach from the screw shaft due to a crack, which could affect implant stability. One unit was distributed in the U.S. (New Jersey); the remaining 43 units were distributed internationally.

Exactech has recalled 596 Equinoxe Core Instrument Kits (model KIT-311X) because the impactor handle may be missing a cross-pin. This defect could affect the handle's stability during surgical use. No injuries have been reported.

Exactech's Equinoxe Ergo Ergo Modular Impactor Handle (model 321-09-05) may be missing an internal cross-pin. This defect could affect the handle's stability or function during surgical use. The recall affects 120 units distributed across the US and nine other countries.

Penner Patient Care, Inc. is recalling certain Penner Pacific Bathing Spa units (Model 860010-1L) because they do not have the required unique device identifier marked on them. This identifier is needed for proper tracking and safety oversight. No injuries have been reported.

Certain Penner Pacific Bathing Spa units (Models 760010-1 and 770010-1) were distributed without a required unique device identifier (UDI) label. This label helps health authorities track and manage medical devices. The FDA has identified 190 affected units by serial number.

Penner Patient Care, Inc. is recalling certain Penner Pacific Bathing Spa models because they do not have the required unique device identifier (UDI) label. This makes it difficult to track the device for safety purposes. No injuries have been reported.

Penner Patient Care, Inc. is recalling certain Penner Pacific Bathing Spa models (390010-1, 390010-X, 390010-2) because they do not have the required unique device identifier. This is a regulatory compliance issue. About 25 units are affected.

Penner Patient Care, Inc. is recalling certain Penner Pacific Bathing Spa units because they do not have the required unique device identifier (UDI) label. This is a regulatory compliance issue. No injuries have been reported.

Certain Penner Pacific Bathing Spa models do not have a unique device identifier (UDI) as required by FDA regulations. This affects 206 units with specific serial numbers distributed nationwide. No injuries have been reported.

Penner Patient Care, Inc. is recalling certain Penner Pacific Bathing Spa units (Model 360020-1P) because they do not have a unique device identifier (UDI) as required by federal regulations. This affects 45 units distributed nationwide. No injuries have been reported.

The device does not bear a unique device identifier.

Certain Penner Pacific Bathing Spa models do not have a unique device identifier (UDI) as required by federal regulations. This affects 643 units with specific serial numbers. No injuries have been reported.

Penner Patient Care is recalling certain Penner Pacific Bathing Spa models because they do not have the required unique device identifier marked on them. This identifier helps track and manage the device if problems arise. No injuries have been reported.

Raz Design mobile shower commode chairs may have improperly engaged rear seat brackets due to a vendor modification. This could cause the seat to become loose or detach during use. The recall affects multiple Raz models nationwide.

A safety feature in the IBA PROTEUS 235 proton therapy system can become disabled, preventing automatic beam shutdown if an external gating device loses signal. This affects only 4 specific units worldwide and may result in incorrect radiation delivery during treatment.

Becton Dickinson discovered that some Luer Slip syringes were accidentally mixed into batches of 10mL Luer-Lok syringes during packaging. This affects product Catalog Number 301029, Lot 5268614, distributed in California and Texas. No injuries have been reported.

Palmetto Gourmet Foods is recalling its Vegetarian Chicken Flavor Ramen Express (3 oz packages) because the product contains Yellow #5 food dye that is not listed on the label. Yellow #5 can cause allergic reactions in sensitive individuals, particularly those with aspirin sensitivity. The affected packages have Best By dates before January 15, 2027.

Palmetto Gourmet Foods' Vegetarian Chicken Flavor Ramen Express contains Yellow #5 food coloring that is not listed on the package label. This undeclared ingredient can cause allergic reactions in people sensitive to Yellow #5. The recall affects packages with a Best By Date before January 15, 2027, distributed across 31 states.

Rosabella brand moringa dietary supplement capsules distributed by Ambrosia Brands LLC may be contaminated with Salmonella, a bacteria that can cause serious illness. The recall affects multiple lots with expiration dates ranging from March 2027 through November 2027. This product was sold nationwide and internationally.

Failed Tablet/Capsule specifications: Red dots inside capsule and melted capsule caused by oxidized Icosapent ethyl, the active ingredient.

The rivets that hold up the swing seat in certain LFTE USA playground swings can fail without warning, causing the seat to fall and potentially injure children. The company has received one report of a child falling from a broken swing. Only swings with model number 999604 and marked with code "LF-65708" are affected.

17 Stories Furniture 14-drawer dressers sold on Wayfair can tip over and trap children if not securely anchored to the wall. The dressers fail to meet federal safety standards for clothing storage units. About 3,000 units in black, white, and brown were sold between September 2023 and January 2026.

LIVEHOM fabric dressers sold on Amazon are unstable and can tip over or trap children if not anchored to a wall. The dressers do not meet federal safety standards for clothing storage units. About 370 units were sold between December 2025 and January 2026.

ProRider bicycle helmets do not meet mandatory U.S. safety standards for impact protection, positioning, and labeling. In a crash, these helmets may fail to protect your head, creating a serious risk of injury or death. The recall affects Economy, Bike Helmet with turn ring, Black Foam, BMX, and Toddler models sold from June 2022 through May 2023.

Kluster magnet chess games contain small loose magnets that can be swallowed by children. When multiple magnets are ingested, they can attract each other inside the stomach and intestines, causing serious injury or death from blockages, twisting, or perforation.

Olympus has identified a mis-wired component in certain ShockPulse-SE Lithotripsy System generators (model SPL-G) that can cause electrical noise in the ultrasonic circuit. This noise may reduce the system's reliability and delay treatment. The recall affects 55 units distributed internationally.