Recalls of medical devices, diagnostic equipment, implants, and surgical instruments.
Showing 3361–3380 of 39,430 recalls
Philips Respironics, Inc.
This device does not indicate for use in patients with respiratory failure.
Baxter Healthcare Corporation
The replacement rechargeable batteries inserted into the Welch Allyn PocketScope handles have the potential to cause a short circuit in the handle, which can lead to exposure to excessive heat and user burns.
Ortho-Clinical Diagnostics, Inc.
a software anomaly allows test results to be reported using Micro Tip and Micro Slide diluent packs that the system treats as expired even when the Use Expired Reagents setting is not enabled if a shelf expiration date is omitted during manual loading. The issue was identified by a customer complaint, in which a CREA Urine test was processed with an RE (Reagent Expired) code, even though the diluent pack was not expired and the use-expired-reagents setting was disabled. This can result in erroneous test results and/or delaying test results.