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Medical Devices Recalls

Medical equipment, implants, and diagnostic devices

38,779 Total Recalls

It was reported that the secondary locking mechanism, and its corresponding components, disassociated from the Specialty Triathlon Tibial Alignment Handle with Secondary Lock Assembly during surgery. Upon further investigation, it was discovered that the weld, which was intended to hold the secondary locking mechanism together, did not meet the weld size specified on the engineering drawing.

Jun 23, 2016 Implants & Prosthetics Nationwide View Details →

The possibility exists for contaminants, in the form of biomass, to develop in the cooling system of Artis systems resulting in damage to the pump system.

Jul 13, 2016 Diagnostic Equipment Nationwide View Details →

The rear gradation scale was screen printed upside down on the flowmeter gauge.

Jun 21, 2016 Diagnostic Equipment Nationwide View Details →

Topcon discovered an anomaly with titration, only when EpM is turned on during the titration process. This event may occur if the user turns on EpM, turns off the Landmark (LM) function (with any EpM supported pattern) and then enters titration mode.

Jul 15, 2016 Other Medical Devices Nationwide View Details →

Due to an error in the 19 Live Display, image reproduction may fail in the examination room and the potential exists for the loss of images immediately after system startup.

Jul 7, 2016 Diagnostic Equipment Nationwide View Details →

Incorrect drill protocol in the Instructions for Use (IFU)

Jul 20, 2016 Implants & Prosthetics Nationwide View Details →

Ortho Clinical Diagnostics has issued a recall of their VITROS immunodiagnostics Estradiol Reagent assay. The firm was made aware of a potential cross-reactivity between the drug Fulvestrant and theVITROS Immunodiagnostic Estradiol Reagent assay. The firm conducted an internal investigation and was able to confirm biased positive (ranging from 1303-4046%) on Estradiol results, obtained from postmenopausal females taking Fulvestrant.

Jul 14, 2016 Diagnostic Equipment Nationwide View Details →

Internal review found that some vials of CD3/CD4/CD45 state that the product contains gelatin. The product does not contain gelatin and should state in buffer.

Jul 18, 2016 Diagnostic Equipment Nationwide View Details →

Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle.

Jul 1, 2016 Implants & Prosthetics Nationwide View Details →

It was reported that the specified lots of the 2.4mm Titanium Locking Screw Self-Tapping with Stardrive Recess 12mm can break between the head and the shaft. This resulted from the neck feature being too close to the StarDrive feature leaving a thin wall between neck and drive.

Jun 28, 2016 Infusion Pumps View Details →

The current construction of the side rail latch may not be able to support the full patient weight and may give way allowing the side rail to abruptly lower and the patient to fall, potentially resulting in harm. To date there has been one report of a related injury.

Jun 14, 2016 Infusion Pumps Nationwide View Details →