Class I - Dangerous
Product coatings require 510K approval.
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Surgical Instruments
🏥 Medical Devices • 6,839 recalls
Class I - Dangerous
Product coatings require 510K approval.
Class I - Dangerous
Product coatings require 510K approval.
Class I - Dangerous
Product coatings require 510K approval.
Class I - Dangerous
Product coatings require 510K approval.
Class I - Dangerous
Product coatings require 510K approval.
Class I - Dangerous
Product coatings require 510K approval.
Class I - Dangerous
Product coatings require 510K approval.
cobas¿ 4800 system z480 instrument. Integrates fully automated total nucleic acid isolation directly from secondary sample tubes.
Roche Molecular Systems
Class I - Dangerous
In rare instances, channel shifted results have been generated with cobas¿ 4800 assays run on v1.1.1 of the cobas¿ 4800 system. Raw data review indicates that, in these cases, all signals are shifted by one channel: channel 1 results report as channel 2, channel 2 results report as channel 3, channel 3 results report as channel 4, and channel 4 results report as channel 1. In the reported
Class I - Dangerous
Product coatings require 510K approval.
Class I - Dangerous
Product coatings require 510K approval.
Class I - Dangerous
Product coatings require 510K approval.
Class I - Dangerous
Product coatings require 510K approval.
Class I - Dangerous
The VP1600 HD Still Capture Image System is recalled due to an anomaly between the software code in the VP1600 console and the communications interface for various keyboard key strokes (Caps lock and Num Lock) which may lock up and requires the user to reboot to continue.
Class I - Dangerous
Product coatings require 510K approval.
Class I - Dangerous
Due to the process deviation, product lots in question may have been released with higher levels of pyrogens than permitted by the specifications for the products.
Class I - Dangerous
Edwards Lifesciences is recalling certain Proplege Coronary Sinus Catheter, model PR9 due to confirmed reports of blood leakage through the hemostasis valve in the introducer that is kitted with the catheter.
Insight Instruments, Inc., Stuart, FL is recalling M.I.S. (Multi-Port Illumination System), Ophthalmic Cannula due to a misclassification of the medical device.
Class I - Dangerous
LifeLiner Stick and Cut Resistant Gloves are being recalled because cases and individual glove packages were mispackaged, with right handed, large sized glove packaging containing left handed, large sized gloves.
Class I - Dangerous
Due to the process deviation, product lots in question may have been released with higher levels of pyrogens than permitted by the specifications for the products.