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U.S. Department of Health and Human Services

Class 2 Device Recall Filters

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 Class 2 Device Recall Filterssee related information
Date Initiated by FirmOctober 15, 2007
Date PostedApril 24, 2008
Recall Status1 Terminated 3 on September 01, 2009
Recall NumberZ-1056-2008
Recall Event ID 45545
510(K)NumberK052110 K842876 K970173 
Product Classification ventilation accessories - Product Code BZD
ProductFilters 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 accessories for sleep therapy and ventilation devices, Respironics, Inc., Murrysville, PA 15668.
Code Information Lot Numbers 071010, 071011, and 071012.
Recalling Firm/
Manufacturer		 Respironics, Inc.
1001 Murry Ridge Ln
Murrysville PA 15668-8550
For Additional Information ContactKatherine dePadua
724-387-7770
Manufacturer Reason
for Recall		Foreign material: Glass fragments may present in the plastic bag material used to ship components.
FDA Determined
Cause 2		Environmental control
ActionThe recalling firm issued a Recall Notification dated 10/18/07 to its customers. Replacement products were to be sent.
Quantity in Commerce20950 units
DistributionThe products were shipped nationwide to medical facilities.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database510(K)s with Product Code = BZD
510(K)s with Product Code = BZD
510(K)s with Product Code = BZD
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