Heart Pump Controller Recall: Abiomed Removes Automated Impella Controllers
Abiomed is removing Automated Impella Controllers due to purge cassette recognition failures that may lead to prolonged delayed in mechanical circulatory support.
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Abiomed is removing Automated Impella Controllers due to purge cassette recognition failures that may lead to prolonged delayed in mechanical circulatory support.
The recalled children’s toys violate the mandatory standard for toys because they contain button cell batteries and the compartments that hold the batteries can be easily accessed by children, posing a deadly ingestion hazard to children. When button cell and coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
The lithium-ion battery in the power banks can explode or ignite, posing fire and burn hazards to consumers.
The lithium-ion battery in the recalled portable sleep machines can overheat if the charger is not compatible with the unit, posing a risk of injury from fire and burn hazards.
The lithium-ion battery in the recalled battery packs can overheat, posing fire and burn hazards to consumers.
The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory safety standards as required by the STURDY Act .
The recalled mattresses violate the mandatory flammability standard for mattresses , posing a risk of serious injury or death from fire.
The helmets in the recalled sets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, retention system, positional stability, labeling and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.
The recalled fuel containers violate the mandatory safety standards for portable fuel containers because they lack flame mitigation devices required under the Portable Fuel Container Safety Act , posing a deadly flame jetting hazard. Furthermore, the methanol container is not child-resistant as required under the Poison Prevention Packaging Act , posing a risk of serious injury or death if the contents are swallowed by young children. The containers also do not comply with the labeling requirements of the Federal Hazardous Substances Act .
The left temple of the recalled smart glasses can overheat during extended use, posing a risk of serious injury or death due to burn hazard.
The recalled mattresses violate the mandatory flammability standard for mattresses , posing a risk of serious injury or death from fire.
The recalled mattresses violate the mandatory flammability standard for mattresses , posing a risk of serious injury or death from fire.
Berlin Seeds, of Millersburg, OH, is recalling 950 lbs of Alfalfa Sprouting Seed because the seed has the potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) and/or Salmonella.
Global Mix Inc. of Middle Village, New York, is recalling niwali Tejocote Capsules (90 capsules, Herbal Supplement) and niwali Tejocote Pieces (90 Day Supply, Herbal Supplement) because FDA analysis has determined that the products appear to be Thevetia peruviana, or yellow oleander. All parts of th
AVID Medical is correcting convenience kits containing recalled Huons Co. sodium chloride ampules.
The cannula sets may exhibit a loose connection between the flexible tubing and the nasal cannula resulting in reduced effectiveness and decreased oxygenation.
GF Blends is recalling Truly AIP All Purpose Flour and Bread Mix and EAT G.A.N.G.S.T.E.R. Flat Bread Pizza Mix listed below due to potential undeclared wheat gluten. People who have celiac disease or a severe gluten intolerance run the risk of adverse health effects or allergic reactions if they con
ROCHESTER, MI– September 18, 2026 –Par Health is voluntarily recalling two lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection 400 mcg/100 mL (4 mcg/mL) to the hospital level. The product is being recalled due to the presence of particulate matter identified as cellulose or stopper materia
Spectra Medical Devices is removing Sodium Chloride Flush products that were manufactured by Huons Co,. Ltd.
Otsuka ICU Medical LLC is issuing a voluntary recall for one lot of 0.9% SODIUM CHLORIDE Injection, USP, 100mL single pack to the user level due to a potential mix-up. The affected lot of 0.9% SODIUM CHLORIDE Injection, USP (NDC: 0990-7984-23 Lot 1042188) may potentially contain the overwrap with la
The fire hose port can come loose and detach, posing a risk of serious injury from choking hazard.
The grounding wire for the grill’s heating element can disconnect and lose fault protection, posing an electric shock hazard.
The saunas contain a bench that can collapse, posing a fall hazard to consumers. The previous recall repair was ineffective; a new repair is now being offered.
During operation the heaters can produce high levels of carbon monoxide (CO), posing a risk of serious injury or death from carbon monoxide poisoning.
The recalled teething toys violate the mandatory safety standard for toys because the silicone strings are smaller and longer than permitted. The silicone strings can reach the back of the throat and become lodged, posing a risk of respiratory distress and a deadly choking hazard.
The internal wire heating elements of the blankets and pads can overheat, posing fire and burn hazards to consumers.
The control board inside the motor of the recalled air conditioners can fail, posing a risk of serious injury or death from fire and burn hazards.
The mattresses violate the mandatory flammability standard for mattresses , posing a risk of serious injury or death from fire.
The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, which may encourage use of an extension cord, posing serious risks of injury or death from shock and electrocution hazards.