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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10 NIOSH Approvals rescinded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5 NIOSH Approvals rescinded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