Rusch Inc RFMD T-Piece With 2 one-way valves & tubing, Ref 395940, Lot***, SINGLE USE ONLY, Qty 1 ea, RUSCH 2450 Meadowbrook Parkway, Duluth, GA 30098***. Carton labeling was similar to individual unit labeling, except for, ***Qty 50 ea. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
RFMD T-Piece With 2 one-way valves & tubing, Ref 395940, Lot***, SINGLE USE ONLY, Qty 1 ea, RUSCH 2450 Meadowbrook Parkway, Duluth, GA 30098***. Carton labeling was similar to individual unit labeling, except for, ***Qty 50 ea.
Brand
Rusch Inc
Lot Codes / Batch Numbers
Catalog No. 395940, Lot numbers: 108273, 109600, 111314, 111229, 113984, 113932, 113931, 112991, 112514, 111588, 111589, 111558, 111557, 117867, 117866, 116471, 116163, 115616, 114992, 116865, 118714, 118055, 118054, 118053, 119421, 120628, 120521, 120021, 120741, 120742, 122619, 122621, 122620, 123017, 123016, 123837, 126217, 125471, 125117, 124069, 126626, 126625, 127052, 127051, 128481, 128322, 127549, 127550, 129360, 129109, 129991, 130186, 130187.
Products Sold
Catalog No. 395940, Lot numbers: 108273, 109600, 111314, 111229, 113984, 113932, 113931, 112991, 112514, 111588, 111589, 111558, 111557, 117867, 117866, 116471, 116163, 115616, 114992, 116865, 118714, 118055, 118054, 118053, 119421, 120628, 120521, 120021,120741, 120742, 122619, 122621, 122620, 123017, 123016, 123837, 126217, 125471, 125117, 124069, 126626, 126625, 127052, 127051, 128481, 128322, 127549, 127550, 129360, 129109, 129991, 130186, 130187.
Rusch Inc is recalling RFMD T-Piece With 2 one-way valves & tubing, Ref 395940, Lot***, SINGLE USE ONLY, Qty 1 ea, RUSCH 24 due to Valve cap may become loose and enter the air circuitry.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Valve cap may become loose and enter the air circuitry.
Recommended Action
Per FDA guidance
Consignees were notified on 2/3/2004 via certified mail and telephone.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026