Getinge’s Maquet/Datascope IABP Devices: Update on Device Failure – Letter to Health Care Providers (updated 08/31/2023; 12/02/2022) |
12/22/2021 |
Possible False RPR Reactivity with BioPlex 2200 Syphilis Total & RPR Test Kit Following a COVID-19 Vaccine - Letter to Clinical Laboratory Staff and Health Care Providers |
12/17/2021 |
UPDATE: Potential Biocompatibility Concerns with NuVasive Specialized Orthopedics’ Precice Devices - Letter to Health Care Providers (updated 6/28/2023) |
12/01/2021 |
Leadless Pacing Systems: Risk of Major Complications Related to Cardiac Perforation During Implantation - Letter to Health Care Providers |
11/17/2021 |
UPDATE: Potential Risk of Infection When Using Heater-Cooler Devices – Letter to Health Care Providers |
10/13/2021 |
UPDATE: Safe Use of Surgical Staplers and Staples - Letter to Health Care Providers |
10/07/2021 |
Left Atrial Appendage Occlusion (LAAO) Devices Potentially Associated with Procedural Outcome Differences Between Women and Men - Letter to Health Care Providers |
09/27/2021 |
Potential for False Positive Results with Abbott Molecular Inc. Alinity m SARS-CoV-2 AMP and Alinity m Resp-4-Plex AMP Kits - Letter to Clinical Laboratory Staff and Health Care Providers |
09/17/2021 |
Potential Risk of Aluminum Leaching with Use of Certain Fluid Warmer Devices - Letter to Health Care Providers |
09/15/2021 |
Stop Using Certain N95 Respirators Manufactured by Shanghai Dasheng - Letter to Health Care Providers |
08/25/2021 |
Stop Using All Eco-Med Ultrasound Gels and Lotions Due to Risk of Bacterial Contamination – Letter to Health Care Providers |
08/18/2021 |
Potential Biocompatibility Concerns with NuVasive Specialized Orthopedics’ Precice Devices – Letter to Health Care Providers (updated 6/28/2023, 12/01/2021) |
07/08/2021 |
Update: FDA No Longer Authorizes Use of Non-NIOSH-Approved or Decontaminated Disposable Respirators - Letter to Health Care Personnel and Facilities |
06/30/2021 |
Sodium Citrate Blood Specimen Collection Tube Conservation Strategies - Letter to Health Care and Laboratory Personnel (updated 01/19/2022) |
06/10/2021 |
Stop New Implants of the Medtronic HVAD System - Letter to Health Care Providers |
06/03/2021 |
Update: FDA Recommends Transition from Use of Non-NIOSH-Approved and Decontaminated Disposable Respirators - Letter to Health Care Personnel and Facilities (updated 06/30/2021) |
05/27/2021 |
Stop Using Certain Syringes and Needles with Needle Safety Devices Manufactured by HAIOU - Letter to Health Care Providers |
05/20/2021 |
FDA Recommends Transition from Use of Decontaminated Disposable Respirators - Letter to Health Care Personnel and Facilities (updated 06/30/2021, 05/27/2021) |
04/09/2021 |
Infections Associated with Reprocessed Urological Endoscopes - Letter to Health Care Providers |
04/01/2021 |
Potential for False Results with Roche Molecular Systems, Inc. cobas SARS-CoV-2 & Influenza Test for use on cobas Liat System-Letter to Clinical Laboratory Staff, Point-of-Care Facility Staff, and Health Care Providers |
03/12/2021 |
Using Ventilator Splitters During the COVID-19 Pandemic - Letter to Health Care Providers |
02/09/2021 |
Genetic Variants of SARS-CoV-2 May Lead to False Negative Results with Molecular Tests for Detection of SARS-CoV-2 - Letter to Clinical Laboratory Staff and Health Care Providers |
01/08/2021 |