ClearanceBrief
Recall Z-1069-2008 ยท BZD Ventilator, Non-Continuous (Respirator)

Respironics, Inc.

Non-continuous ventilator accessories under the following brand names: a) REMStar Pro2 Domestic model number 1020923; b) REMStar Pro M, w/Humid w/Smartcard US model number DS400HS; c) REMStar Pro M w/Smartcard US model number DS400S; d) REMStar Pro/Plus Silencer Cap model number 1005962; e) REMStar Pro/Plus/Auto/Lite Pollen model number 1005964; f) REMStar Pro/Plus/Auto/Lite Pollen SNGL model numb

DateApr 24, 2008 (initiated Oct 15, 2007)
StatusTerminated
ReasonForeign material: Glass fragments may present in the plastic bag material used to ship components.
Root causeEnvironmental control
ActionThe recalling firm issued a Recall Notification dated 10/18/07 to its customers. Replacement products were to be sent.
Quantity20950 units
DistributionThe products were shipped nationwide to medical facilities.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K021861REMSTAR PRO WITH C-FLEX CPAP SYSTEM
Respironics, Inc., Jun 19, 2002
K052110M-SERIES PRO CPAP SYTEM
Respironics, Inc., Oct 20, 2005