The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery.
Other Medical Devices
🏥 Medical Devices • 15,809 recalls
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Philips DXR System, DuraDiagnost 4.1. Stationary X-Ray System.
Philips North America
Potential for collimator to fall as a result of incorrect installation.
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Medline Convenience kits used for various procedures: 1) RHINOPLASTY PACK, Model Number: DYNJ27333F
MEDLINE INDUSTRIES, LP - Northfield
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Brand Name: ID NOW COVID-19 2.0 24T Product Name: ID NOW COVID-19 2.0 24T Model/Catalog Number: 192-000 Software Version: N/A Product Description: Simple Point-Of-Care Device To Detect Sar-Cov-2 Nucleic Acid Targets Component: No
Abbott Diagnostics Scarborough
The impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
Refer to RES
MEDLINE INDUSTRIES, LP - Northfield
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Medline Convenience kits used for various procedures: 1) PAIN PACK, Model Number: DYNJ67577A; 2) PAIN TRIAL PACK, Model Number: DYNJ67576A;
MEDLINE INDUSTRIES, LP - Northfield
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Medline Convenience kits used for various procedures: 1) INTUBATION TRAY, Model Number: MNS10395;
MEDLINE INDUSTRIES, LP - Northfield
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Medline Convenience kits used for various procedures: 1) PRECIP TRAY, Model Number: MNS12590
MEDLINE INDUSTRIES, LP - Northfield
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Due to a software bug, automated dispensing cabinet is unable to calculate countback discrepancies during the issue process, which causes incorrect transaction quantity to be recorded. This bug can also result in the CUBIE opening more times than needed for the transaction to be completed, which may result in a patient receiving more than the intended dose of medication.
stryker Blueprint Mixed Reality Depth Stop Pin, Catalog Number MRUE206; Total Shoulder Arthroplasty
Tornier S.A.S.
Stryker identified an elevated complaint rate related to difficulties using the Blueprint Mixed Reality Guidance Instrumentation system is multifactorial, but in each instance prohibits the system from meeting its intended use. The most commonly reported complaints were related to impaired software functioning, impaired instrumentation functioning, and general difficulties using the product.
MEDLINE ReNewal ENT Coblator II PROcise XP Wand,w/Integrated Cable Suction & Saline (Blue), Item Number REF EICA88720R
MEDLINE INDUSTRIES, LP - Northfield
Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
MEDLINE ReNewal Coblator II ENT Evac 70 Xtra HP,w/Integrated Cable (Blue/Grey), Number REF EICA58740R
MEDLINE INDUSTRIES, LP - Northfield
Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.
Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: TOL DR R PACK
MEDLINE INDUSTRIES, LP - Northfield
Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.
There is a potential for the sterility of the device to be compromised.
FilmArra Pneumonia Panel plus (Pneumoplus), REF: RFIT-LBL-0374
BioFire Diagnostics
Increased risk of control failures and false negative test results with multiplexed nucleic acid test.