INSPIRA AIR BALLOON DILATION SYSTEM 10x40, 1 PK. Airway balloon dilation catheter.
Integra LifeSciences Corp. (NeuroSciences)
Incorrect product packaged in INSPIRA AIR Balloon Dilation System carton.
95,075 total recalls in our database
Integra LifeSciences Corp. (NeuroSciences)
Incorrect product packaged in INSPIRA AIR Balloon Dilation System carton.
Inari Medical - Oak Canyon
Thrombectomy device specifies vessel range of 2.5-6 mm on the pouch, carton, and Instructions for Use rather than the correct vessel range of 3-6 mm, which could incrementally increase the radial force on the artery, which has the potential of vascular complications.
MEDLINE INDUSTRIES, LP - Northfield
A single lot of the ImmunoCard STAT! Crypto/Giardia Test Kit was inadvertently stored in Medline warehouses at temperatures outside of the labeled storage requirements.
Smiths Medical ASD
Pumps may experience Wireless Connection Modules intermittent connection alarms, which will interrupt an active infusion. Interruption or delay of therapy can lead to serious patient injury or death.
Getinge Disinfection Ab
The frequency inverter is not programmed by supplier according to specification which causes the circulation pump to start earlier than expected, resulting in additional wear and tear, earlier than expected, on the axial seal in the pump housing.
Due to a potential open seal in the sterile barrier packaging .
SCIENCE & BIO MATERIALS
Vials of implant bone granules may contain less product then specified on labeling.
Tornier S.A.S.
A software bug in Blueprint version 4.2.1 prevents users from accessing cases initiated in previous versions of the software.
Bausch & Lomb Surgical
In response to an increased number of reports of toxic anterior segment syndrome (TASS) in conjunction with implantation of enVista Aspire and enVista Envy IOLs, and certain enVista monofocal lenses in the U.S.
Getinge Disinfection Ab
The frequency inverter is not programmed by supplier according to specification which causes the circulation pump to start earlier than expected, resulting in additional wear and tear, earlier than expected, on the axial seal in the pump housing.
Due to a potential open seal in the sterile barrier packaging.
Galt Medical
Due to a potential open seal in the sterile barrier packaging.
Integra LifeSciences Corp. (NeuroSciences)
Inadequate weld that can potentially cause the product to disassemble.
Due to a potential open seal in the sterile barrier packaging.
In response to an increased number of reports of toxic anterior segment syndrome (TASS) in conjunction with implantation of enVista Aspire and enVista Envy IOLs, and certain enVista monofocal lenses in the U.S.
Incorrect labeling in which the front red pouch label did not match the actual size of the medical device. The label on the front of the scope incorrectly states 5.0/2.2 while the back label, shipping box and product inside correctly states 5.6/2.8.
Due to a potential open seal in the sterile barrier packaging .
Masco Canada Limited, of Canada
Small amounts of gas can leak from the valve when it is in the open position, posing fire and burn hazards.
Unknown Manufacturer
The candle's glass container can crack or break while the candle is burning, posing a laceration and fire hazard.
Unknown Manufacturer
The hinges on the foldable rear kickstand support leg can crack or break, posing a fall hazard.