EOPA Arterial Cannula, Model Numbers 77422 (22 Fr) and 77418 (18 Fr)
Medtronic Perfusion Systems
š„ Medical Devices Class I - Dangerous
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
All Recalls
92,900 total recalls in our database
BD Pyxis MedStation 4000 AUX, REF 306
CareFusion 303
š„ Medical Devices Class I - Dangerous
Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,
š„ Medical Devices Class I - Dangerous
The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.
š„ Medical Devices Class I - Dangerous
The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.
š„ Medical Devices Class I - Dangerous
Potential for hole in package compromising sterility of the medical kit.
š„ Medical Devices Class I - Dangerous
As a result of a cloud data migration of Patient and Hospital Electronic Systems (PES and HES) reverted to an outdated configuration causing incorrect/inaccurate pulmonary artery (PA) pressure readings.
š„ Medical Devices Class I - Dangerous
The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.
š„ Medical Devices Class I - Dangerous
As a result of a cloud data migration of Patient and Hospital Electronic Systems (PES and HES) reverted to an outdated configuration causing incorrect/inaccurate pulmonary artery (PA) pressure readings.
š„ Medical Devices Class I - Dangerous
Due to incompatibility of bone tamp (Rev A) and bone funnels (Rev C).
š„ Medical Devices Class I - Dangerous
Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.
Select Series Angled Tip Arterial Cannula, Model Number 72422 (22 Fr)
Medtronic Perfusion Systems
š„ Medical Devices Class I - Dangerous
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
BD Pyxis MedStation ES AUX, REF 324
CareFusion 303
š„ Medical Devices Class I - Dangerous
Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,
Otological Ventilation Tube - T-Tube 12mm - Double - Silicone; Product Code: NZ3312-2;
Adept Medical
š„ Medical Devices Class I - Dangerous
Lack of 510(k) clearance.
Otological Ventilation Tube - Donaldson - Double - Blue Silicone; Product Code: NZ3321-2;
Adept Medical
š„ Medical Devices Class I - Dangerous
Lack of 510(k) clearance.
š„ Medical Devices Class I - Dangerous
Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.
ChrisDowa Roller Window Shades
Shaoxingkeqiao Nenghaozhenfang Co. Ltd., of China
š Consumer Products Class II - Moderate
The recalled roller shades have long operating cords that pose strangulation and entanglement hazards to children, in violation of the federal regulations for window coverings. The shades also violate labeling requirements for window coverings.
Children's Holiday Pajama Sets
Unknown Manufacturer
š Consumer Products Class II - Moderate
The recalled children's pajamas violate the flammability regulations for children's sleepwear, posing a risk of burn injuries to children.
GM12 and GMP12 Folding Knives
Unknown Manufacturer
š Consumer Products Class III - Low Risk
The locking mechanism on the folding knives can fail, posing a laceration hazard to the user.
NQDTPBOR Multi-Purpose Helmets
Unknown Manufacturer
š Consumer Products Class II - Moderate
The helmets do not comply with the positional stability, impact, labeling and certification requirements of the mandatory federal safety regulation for bicycle helmets. The helmets can fail to protect the wearer in the event of a crash, posing a risk of head injury.
Teckwe Hair Dryer Brushes
Unknown Manufacturer
š Consumer Products Class I - Dangerous
The handheld hair dryer brushes lack an immersion protection device, posing an electrocution or shock hazard to consumers if the hair dryer brushes fall into water when plugged in. The CPSC has determined that hair dryers not equipped with the integral immersion protection present a substantial product hazard.