95,102 total recalls in our database
Integra identified that the UCHRAP component (Arc Adapter Plate) would not assemble properly to the UCHRAR component (ARC Adapter Ring) of the Compact Head Ring Adapter due to an error in the manufacturing drawing.
Resource Optimization & Innovation
The kits contain an equipment glove component which may contain splits or holes compromising the sterility.
Resource Optimization & Innovation
The kits contain an equipment glove component which may contain splits or holes compromising the sterility.
Resource Optimization & Innovation
The kits contain an equipment glove component which may contain splits or holes compromising the sterility.
Resource Optimization & Innovation
The kits contain an equipment glove component which may contain splits or holes compromising the sterility.
Ortho Solutions Inc is initiating a recall on behalf of UltOS 3.5mm locking screw. The locking thread feature of the screw was not manufactured to specification. As a consequence there is a risk that a screw may not lock onto the plate at the time of primary insertion into the plate and the bone. In the event of this occurring the non functioning screw would need to be replaced with an alternativ
Resource Optimization & Innovation
The kits contain an equipment glove component which may contain splits or holes compromising the sterility.
Resource Optimization & Innovation
The kits contain an equipment glove component which may contain splits or holes compromising the sterility.
Resource Optimization & Innovation
The kits contain an equipment glove component which may contain splits or holes compromising the sterility.
Resource Optimization & Innovation
The kits contain an equipment glove component which may contain splits or holes compromising the sterility.
Resource Optimization & Innovation
The kits contain an equipment glove component which may contain splits or holes compromising the sterility.
Resource Optimization & Innovation
The kits contain an equipment glove component which may contain splits or holes compromising the sterility.
Resource Optimization & Innovation
The kits contain an equipment glove component which may contain splits or holes compromising the sterility.
Beckman Coulter, Inc. is recalling Access Free T3 Reagent Kit because they were filled incorrectly and contain insufficient quantity of reagents in one or more of the pack wells.
Beckman Coulter is recalling MICroSTREP plus 1 and MICroSTREP plus 2 panels because a manufacturing error may lead to antimicrobic degradation and the potential for elevated or false resistant results.
This update is intended to provide a software update for the Syngo RT Oncologist, which is currently running SW version 4.2 or 4.3. The safety-related issues, which were described in the Customer Safety Notice distributed as UFSN-RTT/RTO 4.3 Adaptive Targeting [Auto-registration]. The update contains several important safety and performance fixes.
Resource Optimization & Innovation
The kits contain an equipment glove component which may contain splits or holes compromising the sterility.
Medtronic Inc. Cardiac Rhythm Disease Management
Some Medical Device Identification Cards provided to SureScan pacemaker patients indicate they have a complete Magnetic Resonance (MR) Conditional system, when in fact, not all of their implanted leads have been FDA approved as MR Conditional.
Synthes (USA) Products
Affected lots of Periarticular Aiming Arms and Insertion Handles (Part Numbers 03.120.001, 03.120.002, 03.120.004 and 03.120.005) for the 4.5 mm LCP Proximal Tibia Plates are not able to be secured to the subsequent versions of these devices as intended.
Resource Optimization & Innovation
The kits contain an equipment glove component which may contain splits or holes compromising the sterility.