Colorado recalls

Sold nationwide. 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.

Serious·CPSC·Jun 25, 2026·Treatlife

Sold nationwide. 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.

Serious·CPSC·Jun 25, 2026·Daikin

Sold nationwide. 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.

Serious·CPSC·Jun 25, 2026·ABGA Advanced Trading

Sold nationwide. 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.

Serious·CPSC·Jun 25, 2026·Small Fish

Sold nationwide. 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.

Serious·CPSC·Jun 25, 2026·Carina

Sold nationwide. 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.

Serious·CPSC·Jun 25, 2026·Shield Line

Sold nationwide. 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.

Serious·CPSC·Jun 25, 2026·Veseacky

Sold nationwide. 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.

Moderate·CPSC·Jun 25, 2026·Spector

Sold nationwide. 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.

Serious·CPSC·Jun 25, 2026·Yongkang Ruihe

Sold nationwide. 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.

Serious·CPSC·Jun 25, 2026·Kith

Sold nationwide. Thoratec is recalling three HeartMate products: HeartMate 3 Left Ventricular System kits, System Controllers, and HM 11V Li-ion Backup Batteries. The 11-volt backup batteries can fail. No injuries have been reported.

Serious·FDA·Jun 24, 2026·Thoratec3 products

Sold nationwide. 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.

Moderate·FDA·Jun 24, 2026·Merit Medical

Sold nationwide. Inspire Medical Systems is recalling two implant lead products, the Respiratory Sensing Lead and the Stimulation Lead, because they carry a Use By Date that goes beyond their validated three-year shelf life. The agency says material can degrade past the labeled date, which may lead to unplanned or premature revision surgery. No injuries have been reported.

Moderate·FDA·Jun 24, 2026·Inspire2 products

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.

Moderate·FDA·Jun 24, 2026·BD

Sold nationwide. 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.

Moderate·FDA·Jun 24, 2026·Beta Bionics

Sold nationwide. 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.

Moderate·FDA·Jun 24, 2026·Staar Surgical

Sold nationwide. Medline recalled 30 products, including urethral catheters, catheterization trays, intermittent latex catheters, and medical procedure kits. During an internal review, the company found that some samples did not meet performance specifications, including surface irregularities, connectors that detached early from the catheter funnel, and some catheters with outer diameters outside specification. No injuries have been reported.

Moderate·FDA·Jun 24, 2026·Medline30 products

Sold nationwide. The Mito Red Light Super Mobile near-infrared therapy device contains a lithium-ion battery that may malfunction and catch fire or burst into flames. The device has been distributed worldwide, including across the United States.

Serious·FDA·Jun 24, 2026·Mito Red Light

Sold nationwide. GE HealthCare is recalling three Giraffe OmniBed product lines, about 43,300 units in total, used as infant incubators and warmers. Under certain conditions, such as impact during transport, fasteners holding the canopy soffit beneath the control panel can come loose, and a fastener could fall into the patient compartment. In rare cases, the canopy soffit could become loose or detach, which could potentially injure a patient. No injuries have been reported.

Moderate·FDA·Jun 24, 2026·GE3 products

Sold nationwide. ConMed is recalling 11 AirSeal access port and obturator products used in minimally invasive (laparoscopic) surgery. The recall is for a potential problem that could cause overpressure alerts during procedures. No injuries have been reported, and the products were distributed nationwide and internationally.

Moderate·FDA·Jun 24, 2026·ConMed11 products

Sold nationwide. Stryker identified that some Triathlon Universal Baseplate Size 3 units (lot UZD9IB) were packaged in boxes labeled as Size 4, while Size 4 units (lot TYX7OB) were packaged in boxes labeled as Size 3. This labeling mix-up could result in using the wrong implant size during surgery.

Moderate·FDA·Jun 24, 2026·Howmedica Osteonics2 products

Sold nationwide. Accriva Diagnostics' directCHECK ACT-LR whole blood quality control product (level 2, lot A6DLA001) has incorrect performance range information on its label. This labeling error could lead to misinterpretation of test results if the correct reference range is not known.

Moderate·FDA·Jun 24, 2026·Accriva Diagnostics

Sold nationwide. Medtronic has identified a firmware anomaly in the O-arm O2 Imaging System detector panel that can cause image artifacts during surgical imaging. The issue affects specific serial numbers of the O-arm O2 model BI70002000. No injuries have been reported.

Moderate·FDA·Jun 24, 2026·Medtronic

Sold nationwide. Steris is recalling two surgical lighting systems, HarmonyAIR A-Series and ALYON, totaling about 2,650 units. The plus and minus buttons used to adjust light intensity on the light heads may detach. No injuries have been reported.

Moderate·FDA·Jun 24, 2026·Steris2 products

Sold nationwide. Paint on the light heads of Steris HarmonyAIR A-Series Surgical Lighting Systems may chip or peel. This could potentially affect the lighting system's performance or introduce debris into the surgical field. The FDA has classified this as a Class II recall.

Moderate·FDA·Jun 24, 2026·Steris

Sold nationwide. Medline is recalling 34 convenience and procedure kits because they contain a recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. The adhesive's butyrate tubing may crack during use, making the product unusable for application. No injuries have been reported.

Moderate·FDA·Jun 24, 2026·Medline34 products

Sold nationwide. Philips is recalling two imaging systems used in medical settings, the Allura Xper and MultiDiagnost Eleva, covering 2 product entries. The hand switch button may not fully release after use, which could cause loss of imaging function or unintended radiation exposure and extra contrast injection. No injuries have been reported.

Moderate·FDA·Jun 24, 2026·Philips2 products

Sold nationwide. Arrow is recalling 35 kits and sets that contain lidocaine, bupivacaine, or 0.9% sodium chloride from a supplier that was itself recalled for quality issues. If the sterility of these water-based injectable drugs is compromised, it could lead to serious or life-threatening injuries. No injuries have been reported, and the products were distributed nationwide.

Serious·FDA·Jun 24, 2026·Arrow35 products

Sold nationwide. A software error in certain Automated Impella Controller devices (used to manage left heart support blood pumps) may affect device function. The error affects controllers with software versions 6.0.1, 6.0.2, 6.0.3, 7.1 and above across multiple regions worldwide.

Serious·FDA·Jun 24, 2026·Abiomed

Sold nationwide. Datex-Ohmeda is recalling three infant resuscitation and warmer products, 550 units in total, because a blender knob shaft can loosen. This can cause the system to deliver an oxygen concentration that differs from the level set by the user, which could lead to too little or too much oxygen for the patient. Only units with a specific blender installed during service are affected.

Serious·FDA·Jun 24, 2026·Datex-Ohmeda3 products