At a glance
Respiratory Protective Device Info announcements inform users of changes to the approval status of specific respirator models or to alert about potential counterfeit or misrepresented products.
Previous Years
- CA 2022-1049 – Revocation of Seven Honeywell Int'l. Inc. SAF-T-FIT Approvals Labeled as Sperian Products
- CA 2022-1048 – Effective Immediately: Voluntary Rescission of Supplied Air Monitoring Systems, Inc. Approval
- CA 2022-1047 – A NIOSH-approved respirator cannot be altered to improve fit. Superseded notice NIOSH CA 2021-1037
- CA 2022-1044 – Immediate information for respirator users regarding NIOSH Public Health Emergency (PHE) Approvals issued during the COVID-19 Response and the action to obsolete (phase out) these PHE approvals
- CA 2022-1043 – Effective Immediately: Voluntary Rescission of Pacific PPE Corporation Approvals
- CA 2022-1042 – Effective Immediately: Voluntary Rescission of ALG Health Approvals
- CA 2021-1037 – Updated user instruction information regarding three NIOSH-approved filtering facepiece respirators TC-84A-9298, TC-84A-9308 and TC-84A-9315
- CA 2021-1033R1 – Guidance for respirator users regarding NIOSH Approved surgical N95 filtering facepiece respirators (surgical N95s) exempt from 510(k) pre- market notification in accordance with the Food and Drug Administration regulations at 21 CFR § 878.4040. Supersedes March 2021 version
- CA 2021-1035 – Revocation of Public Health Emergency Approval TC-84A-PH19
- CA 2021-1033 – Guidance for respirator users regarding NIOSH Approved surgical N95 filtering facepiece respirators (surgical N95s) exempt from 510(k) pre-market notification in accordance with the Food and Drug Administration Final Rule published May 17, 2018
- CA 2020-1028 – Information regarding damaged or degraded head straps on previously stockpiled NIOSH-approved filtering facepiece respirators
- CA 2020-1026 – Information regarding Shanghai Dasheng Health Products Manufacture Co., Ltd. (SDH) filtering facepiece respirators (FFRs) with ear loops and labeled as NIOSH-approved
- CA 2018-1006R1 – Self-contained breathing apparatus (SCBA) user information regarding compressed breathing gas containers (cylinders), NIOSH approval holder user instructions, and Department of Transportation (DOT) permit and marking. Revised: Supersedes the August 2018 version
- CA 2018-1006 – Self-contained breathing apparatus user information regarding compressed breathing gas containers (cylinders), NIOSH approval holder user instructions, and Department of Transportation (DOT) permit and marking
Content Source:
National Institute for Occupational Safety and Health