Categories
Resources
Your Recalls
Loading...
Get email alerts when new recalls match your interests.
Undeclared Wheat
May contain small metal fragments from wire mesh sifter.
Potential for a balloon leak in all lots of (CTS-1000) manufactured since August 2014.
In combination with the Batch Programming option (only) for programming samples, the hand-held barcode scanner unexpectedly skips sample cup positions within a sample tray. This issue only occurs when using the Batch Programming option; all other sample programming options function as intended.
Advanced Sterilization Products (ASP) is recalling the Tyvek Rolls with STERRAD Chemical Indicator because they were shipped to customers after its expiration date of May 18, 2013.
Product distributed without 510(k) approval
A small piece of the stylet sheath has the potential to shear off upon removal of the stylet from the tracheal tube.
The firm is recalling three batches (FP14A09, FP14A10, FP14A11) of SpermMAR IgA test due to new formulation causing the motility of sperm cells to reduce in certain samples when the new bead solution was added.
One unit from a demo lot of POWERFLEX PRO PTA Dilatation Catheter was left at a hospital and was not sterilized.
A single lot (11121171) of Flyte Toga Peel-away X-Large (catalog number 0408-830-100) was labeled with an incorrect expiration date of 2412-12-01. The correct expiration date should have read 2014-12-01.
Shaft breaks so that adequate patient specimen sample cannot be obtained.
Printed mark on the trocar intended to indicate a 5cm distance from the distal tip of the needle is actually located 4cm from the distal tip of the needle.
Two lots of the Anti-Lambda APC-H7 antibody are contaminated with CD38 antibody.
Sp02 and/or Non Invasive Blood Pressure (NBP) alarms may become disabled without visual notification
In May 2013, the original recall was initiated due to complaints the Hand Switch for the Electric Pen Drive was not labeled correctly, and the on and lock labels were interchanged.
The stopper of the 10mL BD Luer-Lok syringe is not properly seated in the syringe.
An ECG procedure time stamp is incorrect, due to a software error in the McKesson Cardiology ECG Management with software versions 13.1 and 13.1.1.
One lot of CD8 PE is contaminated with CD4 FITC and may cause an unexpected staining pattern and incorrect patient data.