New Mexico recalls

ICU Medical's Tego Connector needle-free access devices have a silicone seal that may bulge, separate, or tear. This defect can cause fluid leaks, blockages, inability to draw or inject medication, and potential exposure to contamination or air in the bloodstream during hemodialysis or IV therapy.

RayStation versions 17.0.0 and 17.0.1 have a software error that prevents dose calculations from updating properly when certain regions of interest are modified. This can occur when regions have no contours but include material overrides or are marked as Bolus, Fixation, or Support types. Users may not see updated radiation doses after making changes.

RayStation version 2024B has a software issue where calculated radiation doses may not update correctly when certain regions of interest (ROIs) are modified. This affects ROIs without contours that have material overrides or are classified as Bolus, Fixation, or Support types. Clinics using this version should verify their dose calculations are accurate.

RayStation radiation therapy planning software versions 2024A SP1 and 2024A SP2 have a bug that prevents dose calculations from updating correctly when certain regions of interest (ROIs) are modified. This affects ROIs without contours that have material overrides or are classified as Bolus, Fixation, or Support types. If changes are made to these ROIs, the system may not recalculate doses as intended.

RaySearch's RayStation radiation therapy planning software version 10B SP1 has a flaw where calculated radiation doses may not update correctly when certain regions of interest are modified. This affects regions with no contours that have material overrides or are classified as Bolus, Fixation, or Support types. Clinical staff may unknowingly rely on outdated dose calculations.

RayStation radiation therapy treatment planning software (versions 14.0.0, 15.0.0, and 15.1.3) may not properly update calculated radiation doses when certain regions of interest are modified. This can occur when regions have no contours but have material overrides or are classified as bolus, fixation, or support types. Changes to these regions may not trigger the dose recalculation as intended.

RayStation versions 12A, 12A SP1, and 12A SP2 contain a software bug that prevents dose calculations from updating properly when certain regions are edited. This affects only specific region types (Bolus, Fixation, Support) with no contours that have material overrides. Users may not see updated radiation doses after making changes.

RaySearch RayStation/RayPlan radiation therapy planning software (versions 11B through 11B SPT1) has a bug that prevents dose calculations from updating correctly when changes are made to certain regions of interest with material overrides or specific geometry types. This could result in treatment plans using outdated radiation dose calculations.

RaySearch Laboratories identified a software bug in RayStation/RayPlan versions 11.0.0 through 11.0.4 (11A, 11A SP1, SP2, SP3) used for radiation therapy treatment planning. When certain regions of interest have no contours but have material overrides or are classified as Bolus, Fixation, or Support types, the software fails to recalculate radiation doses correctly if you modify or remove the material override. This could result in outdated or incorrect dose calculations being used for treatment planning.

RaySearch Laboratories' RayStation/RayPlan version 10B has a software issue that can prevent proper recalculation of radiation therapy doses when certain regions are modified. This affects specific treatment planning scenarios where regions have no contours but have material overrides or are classified as Bolus, Fixation, or Support types. Stale dose calculations may be used instead of updated ones.

Zydus Pharmaceuticals is recalling Icosapent Ethyl 1-gram capsules because some bottles may contain capsules that have lost potency (strength) due to leakage and oxidation. This means the medication may not work as intended. The recall affects specific lot numbers expiring in February and April 2027.

Specialty Process Labs is recalling one lot of Thyroid, USP (an active pharmaceutical ingredient used in manufacturing) because it does not meet strength standards. The affected lot may contain less active ingredient than labeled, which could affect the potency of products made with it.

Rising Pharmaceuticals is recalling Furosemide Tablets, USP 40 mg (a water pill used to treat swelling and high blood pressure) because some bottles may contain a foreign substance. The affected lot is FUB125042G with an expiration date of May 2027. This recall affects 4,212 bottles distributed nationwide.

Cipla USA is recalling Diclofenac Sodium Topical Gel 1% (batch XHBG, expiring 08/31/2027) because it failed to meet required pH specifications during quality testing. The gel may not work as intended or could cause skin irritation. No injuries have been reported so far.

Mikario Trading's 5-in-1 convertible baby gyms can obstruct an infant's breathing because the floor mat violates safety standards for infant cushions. The pink gyms, sold on TikTok Shop, convert from an activity center to a tummy-time mat and include a toy bar and plush toys. About 500 units were sold between May and October 2025.

Iristar Minoxidil Spray Bottles sold on Amazon contain minoxidil but lack child-resistant packaging required by law. A young child who swallows the contents could suffer serious injury or death. No injuries have been reported so far.

Cumbor retractable safety gates sold online have a gap between the gate and floor that allows a child's torso to fit through, creating a serious risk of entrapment and injury. About 4,520 units were sold online starting in September 2025. No injuries have been reported yet.

Vndueey Magnetic Men toy sets contain loose magnets that can separate and be swallowed by children. When multiple high-powered magnets are ingested, they can attract each other inside the digestive system and cause serious internal injuries, including intestinal perforation, blockage, and blood poisoning.

Based Online Fidget Magnet Ball Toy Sets contain loose high-powered magnets that can be swallowed by children. When multiple magnets are ingested, they can attract each other inside the digestive system, causing serious injuries including intestinal perforation, blockage, and potentially death.

Topkay torch lighters sold on Amazon lack required child-resistant safety features, creating a risk of serious burns or fire. About 7,500 black two-packs labeled "Honest" were sold between September and October 2025.

Gagaku ice cream shop toy playsets sold on Amazon contain high-powered magnets that can loosen and detach. If a child swallows these magnets, they can attract each other or metal objects inside the digestive system, causing serious injury including intestinal perforation, blockage, blood poisoning, or death.

Yetonamr Pull String Teething Toys have silicone strings that are smaller than safety standards allow. These strings can lodge in a child's throat and cause serious choking, breathing problems, or death. CPSC has received 32 reports of choking incidents.

The power cord on certain Matrix Retail and Vision treadmills can become loose where it connects to the machine, creating a fire hazard. About 47,000 treadmills are affected, manufactured between June 2007 and January 2024. The company has received 27 reports of overheating at the connection, though no injuries have occurred yet.

Academy Sports + Outdoors is recalling Magellan Odyssey Rocker Chairs sold between September and October 2025 because the chair legs can break. This poses a risk of falls and injury. The chairs have a metal frame with mesh backrest and were sold in charcoal, navy, olive green, and teal colors.

Angry Orange Enzyme Stain Remover products may contain Pseudomonas aeruginosa bacteria, which can cause serious infections in people with weakened immune systems, lung conditions, or external medical devices. The bacteria can enter the body through inhalation, eyes, or breaks in the skin. People with healthy immune systems are typically not at risk.

Certain batches of syringes in ICU Medical's Portex Spinal Tray may have cracks in the syringe collar. This defect can prevent the syringe from working properly, cause repeated blood draws, or lead to blood leakage during arterial blood sampling or fluid delivery.

ICU Medical Inc. is recalling specific lots of Pulsator Arterial Blood Sampling Kits because some syringes have cracks in the collar. This crack can cause blood to leak during sampling, delays in blood draws, or the need to repeat the procedure.

Thoratec CentriMag blood pump components used in acute circulatory support and ECMO systems may not lock securely into the motor. If the pump fails to lock properly, the system may not generate an alarm, which could delay critical heart support or cause serious complications.

Medtronic has recalled certain Abre Venous Self-Expanding Stents due to a manufacturing issue with the stent material (Nitinol) that can cause the stent to be smaller than intended when deployed. This reduced size may result in the stent moving out of position after placement.

Intuitive Surgical is recalling certain da Vinci SP Access Port Kits because the sterile trays may develop cracks during storage or handling. A cracked tray could allow bacteria or other contaminants to enter, compromising the sterile field during surgery. No injuries have been reported.