A defect in the seal of the Gatorade pouch contained in kits caused the pouch to leak within a limited portion of the kit.
Surgical Instruments
🏥 Medical Devices • 6,839 recalls
A defect in the seal of the Gatorade pouch contained in kits caused the pouch to leak within a limited portion of the kit.
A defect in the seal of the Gatorade pouch contained in kits caused the pouch to leak within a limited portion of the kit.
A defect in the seal of the Gatorade pouch contained in kits caused the pouch to leak within a limited portion of the kit.
Hyalomatrix products are susceptible to degradation as a result of the decomposition of PVC in the packaging material during sterilization, which resulted in degradation of the film. Over the long term it is possible that product integrity may be compromised.
Product pouch label may not easily identify the lot number, expiration date and associated symbols..
Product pouch label may not easily identify the lot number, expiration date and associated symbols..
Product pouch label may not easily identify the lot number, expiration date and associated symbols..
Devices were found with a sterile breach (puncture) in the pouch from a sort of 8,064 packaged devices.
During long-term storage (i.e. military depot), the interaction of stagnant water and dissimilar metals in the plumbing of the P2131 device produces deposits in the water system that can potentially interfere with the rear sight gauge and / or the water liquid level switch.
Product pouch label may not easily identify the lot number, expiration date and associated symbols..
Specific da Vinci X Surgical Systems (IS4200) were shipped with defective Arm Controller Joint (ACJ) boards that were found to have a high rate of failure due to a defective component.
The recalling firm has received complaints related to increased resistance encountered when introducing the CVC over the spring wire guide. This may lead to procedural delay, and there may be need of medical intervention by exchanging the catheter for another CVC catheter.
Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2", REF 142542 Product Usage: general surgical scissors
Teleflex Medical Europe
The incorrect plastic was used to manufacture the handles of these shears, which causes the handles to melt if sterilized.
The supplier of Drainer(R) centesis catheters notified Vascular Solutions, Inc. that there is a potential for certain production lots to contain unsafe levels of bacterial endotoxins.
The catheter alignment arrow printed onto the strain relief is not aligned with the detachment feature of the catheter connector, resulting in the potential for the catheter to be attached to the controller in the detach orientation. In this orientation, the catheter is not securely attached to the controller and may be partially (~1cm) ejected from controller.
A shipment to Guadeloupe suffered a temperature excursions up to 47.8¿C, exceeding the acceptable limits. After detection of the issue, Global Supply Chain QA asked the bioM¿rieux distributor in Guadeloupe to put products in quarantine in July 2017; After several reminders, the distributor informed in November 2017 that products were delivered to customers.
Bardex Lubricath 3-Way 75cc Continuous Irrigation Foley Catheter (Creevy), 22Fr. Rx (01267522)
C.R. Bard
Foley Catheter with Incorrect Retainer Cap Print
Reports of incorrect priming volume due to manufacturing with incorrect tubing.
IFU contained an automated cleaning process for the VerteLP Instrument Tray that was not validated