ClearanceBrief
Recall Z-1076-2008 ยท BZD Ventilator, Non-Continuous (Respirator)

Respironics, Inc.

Non-continuous ventilator accessories under the following brand names: a) RP-BIPAP Flow Pick-Up Tube Kit model number 332185; b) RP-BIPAP M Series Keypad model number 1038122; and c) RP-BIPAP Pro 2 /Plus Tubing Kit model number 1020358. Filter, mask, and/or accessories for sleep therapy and ventilation devices, Respironics, Inc., Murrysville, PA 15668.

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

K011714BIPAP PRO BI-LEVEL SYSTEM
Respironics, Inc., Jun 28, 2001
K052110M-SERIES PRO CPAP SYTEM
Respironics, Inc., Oct 20, 2005