New Mexico recalls

Ajanta Pharma USA Inc. is recalling one lot of fenofibrate 200 mg capsules due to manufacturing quality deviations discovered during inspection. The affected lot (PA02216, expiring 12/2029) was distributed nationwide.

MAJOR Pharmaceuticals is recalling Methylergonovine Maleate Tablets, USP, 0.2 mg due to subpotency — meaning the tablets contain less active ingredient than labeled. The affected lots were distributed nationwide. This is a prescription medication used to control bleeding after childbirth.

Revival Animal Health is recalling several canine and goat milk replacer products because they contain inconsistent levels of vitamin D—some too low, some too high. Dogs fed these products may develop serious health problems ranging from vomiting and weakness to bone deformities (rickets in puppies) or kidney damage (from excess vitamin D). Two cases of rickets have been reported so far.

Lehi Valley Trading Company recalled 624 units of High Valley Orchard Chocolate Covered Raisins (15 ounce packages) because they contain undeclared peanuts. The affected product has lot #0160933 and a best-by date of January 23, 2027. A temporary breakdown in production and packaging processes caused the contamination.

Treatlife smoke and carbon monoxide detectors can fail to sound an alarm when smoke or fire is detected. These white, circular detectors are powered by AA batteries and were sold on Amazon. The failure to alert poses a risk of serious injury or death from smoke inhalation or burns.

Certain Amana brand window and through-the-wall air conditioners and heat pumps can experience a ground fault that leaves the heating element energized even after the unit is turned off. This poses a risk of fire or burn injury. One report of plastic melting on a unit has been received, though no injuries have occurred so far.

Honlyne LED party favors sold on Amazon contain button cell batteries in compartments that children can easily access and swallow. Swallowing these batteries can cause serious internal injuries, chemical burns, and death.

Small Fish Montessori Busy Board toys (model 2512JX02) contain magnets that can detach and be swallowed by children. When multiple magnets are ingested, they can attract each other inside the digestive system, causing serious injury or death from intestinal perforation, blockage, or infection.

These light-up sneakers contain coin batteries that children can easily access and swallow. Ingesting these batteries can cause serious internal burns and other life-threatening injuries. The sneakers lack required safety warnings and do not meet federal battery safety standards.

MedPride Baby Oil bottles do not have child-resistant caps as required by law. Young children can open the bottle and swallow the oil, which contains petroleum distillates that can cause serious poisoning, chemical pneumonia, and potentially fatal lung damage.

The Lomi Roll-On Waxing Kit (models LOMB2003PK and LOMB2004PK) does not meet safety standards for flammability and presents a risk of burns or fire. These handheld wax warmers were sold online through Amazon from October 2020 through January 2026. About 14,700 units are affected.

The lithium-ion battery in the Super Off-Road 12,000 mAh Solar Wireless Power Bank can swell and overheat, creating a burn hazard. The company has received two reports of battery swelling. About 7,400 units were distributed as promotional items between January 2019 and December 2023.

Yamazuki's Sunderwell brand youth ATVs (model XW-A17) sold online lack brake lights, making them harder for other vehicles to see. This visibility gap increases the risk of crashes and serious injury. About 200 units were sold between October and December 2025.

Kith Retail recalled children's loungewear sets in black and red plaid print because they don't meet federal flammability standards for children's sleepwear. The pajamas pose a risk of serious burn injuries. The sets were sold at Kith stores and online from December 2025 through January 2026.

The HeartMate 11 Volt Lithium Ion Backup Battery, a critical component of the HeartMate 3 System Controller, can fail to provide emergency power when needed. The backup battery is designed to supply at least 15 minutes of emergency power if the main power source fails. Battery failures could prevent the system controller from operating during power loss.

The HeartMate 3 System Controller, which powers and monitors left ventricular assist devices (LVADs), may experience failures in its 11-volt backup battery. This backup battery is critical for emergency power when other power sources are unavailable.

Merit Medical Systems' Splashwire Hydrophilic Guide Wire — used by doctors in vascular procedures — has been recalled because some product pouches were not sealed properly. Unsealed pouches can allow contamination or damage to the sterile device before use.

Inspire Medical Systems' Model 4063 stimulation leads are labeled with expiration dates that extend beyond their actual three-year shelf life. If a lead is used after its true expiration date, the material may degrade and could require unplanned revision surgery. A small number of units (10 total) have been affected worldwide.

Inspire Medical Systems' Respiratory Sensing Lead (Model 4340) was labeled with expiration dates that extend beyond the validated three-year shelf life. If the device is used after its actual expiration date, the material may degrade and could require unplanned revision surgery.

BD Connecta BD Luer-Lok 360 stopcocks used to administer IV fluids and medications may have a connection problem at Port C. When a plastic luer-lok syringe is attached, the connection may over-thread or continue spinning instead of tightening securely, making it feel unstable.

A firmware bug in the iLet Bionic Pancreas can cause the lock screen to fail to unlock when users slide the unlock slider. When this happens, users become stuck on the lock screen and cannot change insulin cartridges or enter meal information. The pump will continue delivering insulin until the cartridge empties and the battery drains, which may lead to high blood sugar.

Staar Surgical's ICL Calculation Software Version 8.00 contains a coding error that can produce incorrect implantation orientation diagrams for toric intraocular lenses. The error occurs when multiple toric lens calculations are generated for the same eye between April 13–16, 2026. An incorrect diagram could lead to improper lens alignment during surgery.

Medline identified that certain surgical procedure kits containing catheters did not meet quality standards. Some kits had catheters with surface irregularities, connectors that could detach prematurely, or catheters that were the wrong size.

Medline identified that samples of several medical procedure kits did not meet quality specifications. Issues included rough catheter surfaces, connectors that detached prematurely, and catheters with incorrect outer diameters. These kits are used in eye and throat surgical procedures.

Medline identified that samples of several medical procedure kits did not meet performance standards. Issues included irregular catheter surface finish, premature connector detachment, and catheters with incorrect outer diameter.

Medline Industries identified that certain batches of medical procedure kits used in gynecological surgeries did not meet quality standards. The kits contained catheters with surface irregularities, connectors that could detach prematurely, and sizing issues that could affect proper function during procedures.

Medline identified that certain D and C Pack and catheter kits did not meet quality specifications. Issues found include surface irregularities on catheters, connectors that detached prematurely from the catheter funnel, and catheters with incorrect outer diameter. The affected kits were distributed worldwide.

Medline identified that samples of its medical procedure kits did not meet quality standards. The catheter components had surface irregularities, connectors that detached prematurely, and in some cases incorrect outer diameters.

Medline identified quality issues in representative samples of its Pelvic Lap Pack medical procedure kit (SKU DYNJ53820B). Problems include surface irregularities on the catheter, premature detachment of the catheter connector, and instances where the catheter diameter fell outside specification. A total of 20 units were affected.

Medline found that samples of several obstetric and gynecological procedure kits did not meet quality standards. The issues include surface irregularities on catheters, connectors that detached prematurely from catheter funnels, and catheters with diameters outside acceptable specifications.