Wyoming recalls

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.

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.

Advanced Bionics is recalling certain Sky CI M90 Sound Processors because the label on the package does not match the product inside. Two units with specific serial numbers (249596 and 249603) are affected. No injuries have been reported.

Vascutek vascular repair grafts (Gelsoft Plus and Gelweave models) were labeled with expiration dates that are too long. The shelf life was incorrectly calculated from the packaging date instead of the gel treatment date. This means some devices may expire sooner than the label states.

Diagnostica Stago's STA Liatest Free Protein S testing kits (model REF 00516) may produce inaccurate results, potentially underestimating free protein S levels in normal patient samples. This affects specific lot numbers distributed nationwide and internationally. No injuries have been reported.

Esaote has identified a weakness in the probe body on a specific production batch that may cause liquid to leak from the cable connection area. Five units with specific serial numbers were distributed in North Carolina and Texas.

Olympus has recalled its Single Use Biopsy Valve (model MAJ-1218) used during endoscopy procedures. Small rubber fragments may detach from the valve during use, potentially entering the patient's body. No injuries have been reported, but the risk prompted this recall of about 25,500 affected valves.

Olympus has recalled the MAJ-210 single-use biopsy valve (a device that attaches to endoscopes to prevent fluid backflow) because rubber fragments may detach during use. The recall affects all lot numbers of this product sold nationwide. No injuries have been reported to date.

Datascope Corp. has identified that the battery runtime and cycle specifications in the instruction manual for the CS300 IABP (intra-aortic balloon pump) device need to be corrected. The device itself is safe to use, but the written specifications may not accurately reflect actual battery performance.

Datascope Corp. identified that the battery runtime and cycle specifications in the instruction manual for the CS100 IABP (intra-aortic balloon pump) device are incorrect and need to be updated. The device itself is not defective, but users may rely on outdated battery information.

Aesculap Inc. is recalling certain MINOP Trocar 150mm surgical instruments (model FF399R) because the shaft may be longer than intended. This surgical tool is used during minimally invasive procedures. No injuries have been reported so far.

Siemens Healthcare Diagnostics recalled its Atellica CH Urine Albumin test kits because they may report falsely low results for high-protein urine samples. If a sample contains more than 40.0 mg/dL of albumin, the test may incorrectly show a value between 6.2 and 40.0 mg/dL instead. This affects all lot numbers of Material Number 11537225 distributed worldwide.

B. Braun Medical Inc. recalled certain winged infusion sets used to expand tissue expanders because the needle tips may be dull, blunt, or break during use. This could make it difficult to insert the needle or cause it to break inside the body. No injuries have been reported.

B. Braun Medical Inc is recalling certain 21-gauge winged infusion needles used to expand tissue expanders. The needle tips may be dull, blunt, or break during use, which could make the device difficult or impossible to use properly.

B. Braun's 21G winged injection needles used for tissue expander procedures may have dull, blunt, or broken needle tips. This can make the needle difficult to advance during use. The issue affects specific lot numbers with expiration dates through September 2032.

Staar Surgical EVO+ Visian Toric Implantable Collamer Lenses (Model VTICM5) were labeled as 12.1 mm but are actually 12.6 mm in length. The larger size can cause the lens to sit too high in the eye, potentially reducing eye drainage and increasing eye pressure, which may lead to discomfort, vision problems, or the need for lens removal.

The Olympus ShockPulse-SE Lithotripsy System generator (model SPL-G) may fail to recognize its transducer and remain in a blinking waiting state. This can happen if the transducer plug or generator receptacle becomes damaged. The device is used in medical settings to break up kidney stones and similar calculi.

The Olympus ShockPulse-SE Lithotripsy System, used to break up kidney stones and similar calculi, may experience problems where the generator remains in a blinking phase and fails to recognize the transducer. This can happen if the transducer plug or generator receptacle becomes damaged. No injuries have been reported.