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.
2026 Respiratory Protective Device Info Notices
- CA 2026-1110 – Effective Immediately: Voluntary Rescission of three approvals for Masprot S.C., EI. LTDA
- CA 2026-1108 – Effective Immediately: Voluntary Rescission of four approvals for PIP Global Holdings, Inc
- CA 2026-1107 JCI – Effective Immediately: Voluntary Rescission of one approval for Jahan Company t/a IREMA Ireland
- CA 2026-1106 – Effective Immediately: Voluntary Rescission of one approval for Reusable Respirators, LLC
- CA 2026-1105 – Effective Immediately: Voluntary Rescission of one approval for Industrias Saver
- CA 2026-1104 – Effective Immediately: Voluntary Rescission of one approval for D. Wheatley Enterprises, Inc.
- CA 2026-1103 – Effective Immediately: Voluntary Rescission of 17 approvals for RPB Safety, LLC
Previous Years
- CA 2025-1102 – Effective Immediately: Voluntary Rescission of 101 approvals for Honeywell International, Inc.
- CA 2025-1101 – Effective Immediately: Voluntary Rescission of one approval for Pure Environments by Shatkin First, Inc.
- CA 2025-1099 – Effective Immediately: Voluntary Rescission of 16 approvals for Interspiro USA, Inc.
- CA 2025-1098 – Effective Immediately: Voluntary Rescission of 134 approvals for 3M Scott Fire & Safety
- CA 2025-1097 – Effective Immediately: Voluntary Rescission of 801 Approvals for 3M Company
- CA 2025-1096 – Effective Immediately: Voluntary Rescission of 95 Approvals for 3M Company
- CA 2025-1095 – Effective Immediately: Voluntary Rescission of one ivWatch, LLC Approval
- CA 2025-1094 – Effective Immediately: Voluntary Rescission of Four Kimberly-Clark Corporation Approvals
- CA 2025-1093 – Effective Immediately: Voluntary Rescission of Three Venus Safety & Health Pvt., Ltd Approvals
- CA 2025-1092 – Effective Immediately: Voluntary Rescission of One Global Safety First, LLC Approval
- CA 2025-1091 – Effective Immediately: Voluntary Rescission of Four Avon-International Safety Instruments, Inc. Approvals
- CA 2025-1090 – Effective Immediately: Voluntary Rescission of two Aidway Personal Care Product, Inc. Approvals
- 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
About This Page
Published: April 23, 2025
Updated: March 4, 2025
This page was last updated on this date. Updates may include minor edits, image changes, or other modifications to page content.
Reviewed: March 4, 2025
The information on this page was last reviewed by subject matter experts to ensure accuracy.