ClearanceBrief
Recall Z-1056-2008 ยท BZD Ventilator, Non-Continuous (Respirator)

Respironics, Inc.

Filters under the following brand names: a) filter std incoming 7100 CPAP qty 1 model number 1039618; b) filter reusable PLV 2/pkg model number 35220; c) LX UL Fine Filter 2 pack model number 1006193; d) RP-M Series Ultrafine Filters 6 pack model number 1029331; e) RP Vision OM Reg Filter (ASCO) model number 1007547; and f) REPL Filters package of 4 model number 929-4. Filter, mask, and/or acces

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

K052110M-SERIES PRO CPAP SYTEM
Respironics, Inc., Oct 20, 2005
K842876PORTABLE LIFECARE VENTILATOR PLV-102
Lifecare Services, Inc., Aug 29, 1984
K970173MODEL 1700 TRANQUILITY BILEVEL SYSTEM
Healthdyne Technologies, Inc., Apr 16, 1997