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Certified Product Investigation Process (CPIP) - FY12

Objective

  • To maintain the quality of NIOSH Certified respiratory protective devices used in the field by investigating and resolving reports of product nonconformance issues in a timely manner.
  • Respond to all reports of nonconforming respirators.
  • Evaluate corrective actions taken by approval holders to ensure conformance to the criteria listed in 42 CFR, Part 84.

Applicable Standards

  • None

Key Partners

  • NFPA
  • IAFF
  • SEI
  • MSHA
  • OSHA
  • FDA
  • EPA

Stakeholders

  • Respirator Users
  • Enforcement Agencies
  • Emergency Responders
  • Respirator manufacturers worldwide

Project Scope


  • Communicate and interact with manufacturers and distributors world-wide.
  • Respond to various levels of demand.
  • Establish and enforce accountability for nonconformances.

Milestones

  • None

Outputs

  • 15 CPIP investigations opened (24 for FY11)
  • 10 CPIP investigations completed (19 for FY11)
  • 4 Firefighter reports generated
  • 10 NIOSH Approvals rescinded
  • 6 User Notices issued
  • 5 NIOSH Approvals rescinded
  • 2 Stop-sale requests

Outcomes

  • Ensure that NIOSH approved respiratory devices continue to meet or exceed the criteria on which the approval was based
  • Removal of CSE SR-100 from production and advances in cold start retraining
Page last updated: April 17, 2012
Page last reviewed: April 17, 2012
Content Source: National Institute for Occupational Safety and Health (NIOSH)
National Personal Protective Technology Laboratory