Devon Light Gloves contain splits or holes compromising the sterility
Other Medical Devices
๐ฅ Medical Devices โข 15,809 recalls
Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Bausch & Lomb SofPort Advanced Optics Aspheric Lens
Bausch & Lomb Surgical
Haptics breaking during lens loading and insertion.
Devon Light Gloves contain splits or holes compromising the sterility
Safety PICC Insertion Tray with Chloraprep OneStep - Model #5026CL-9 - 12 pr case. Packaged for Physician use only.
Custom Healthcare Systems
An INCORRECT item number is packed within the OUTSIDE "PIGGYBACKED" PACKAGE. The interior sealed STERILE KIT is correct and NO adverse issues affect that part of the item. The NON-STERILE OUTSIDE "PIGGYBACKED" PACKAGE mistakenly contains ITEM #8881579121 - Syringe prefilled, Saline Flush, 09% Sodium Chloride and is a NONSTERILE PRODUCT that CANNOT BE DROPPED INTO THE STERILE FIELD.
Devon Light Gloves contain splits or holes compromising the sterility
Devon Light Gloves contain splits or holes compromising the sterility
Devon Light Gloves contain splits or holes compromising the sterility
Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
1X1 Cleaving Tiles; The Fiber Cleaver is a reusable and sterilizable tool used to score the outer jacket on Endostat and SureFlex Fibers. The tool is a one piece pencil-like design with a sharpened blade at the end. The Fiber Cleaver is a SureFlex TM Reusable Laser Lithotripsy fiber and EndoStat fiber accessory. The Fiber Cleaver does not come in direct contact with the patient.
American Medical Systems Innovation Center - Silicon Valley
validation data related to cleaning instructions and sterilization methods and the methods defined in instructions for use (IFU) for the Sureflex Reusable Fibers and the Reusable Stripper and Cleaver Accessories do not meet the new guidance on qualifying reusable products
Silhouette Lift brochure Silhouette Sutures are for use in midface suspension surgery to fixate the cheek subdermis in an elevated position.
Silhouette Lift
Silhouette Lift is recalling the Silhouette Suture brochure because it does not include a complete list of risks and side effects. Therefore, it can potentially mislead the patient regarding the safety of the product.
Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
GE Healthcare Precision RXi 23A/32A Analog System
GE Healthcare
A reported incident of a monitor that fell from the suspension. A fall of a monitor could result in an injury to a patient or operator. Recall affects the single and dual LCD monitor suspensions used on Precision 500D Classical R & F system, Precision RXi 23A/32A Analog System, Precision RXi Digital system and Precision MPi fluoroscopic imaging systems.
Devon Light Gloves contain splits or holes compromising the sterility
Devon Light Gloves contain splits or holes compromising the sterility
Multiaxial screws may not meet internal requirements related to fatigue strength. Compression testing result and surface treatment are out of specification.
GE Healthcare Precision RXi Digital system
GE Healthcare
A reported incident of a monitor that fell from the suspension. A fall of a monitor could result in an injury to a patient or operator. Recall affects the single and dual LCD monitor suspensions used on Precision 500D Classical R & F system, Precision RXi 23A/32A Analog System, Precision RXi Digital system and Precision MPi fluoroscopic imaging systems.
Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Devon Light Gloves contain splits or holes compromising the sterility