FDA Recall Terminated

Hyperinflation Circuit, consisting of a 2.0 L breathing bag, pressure monitoring tube, oxygen supply tubing, sideport connector with adjustable bleed valve and ported elbow; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83120

Recall: Z-0036-04 · Initiated September 10, 2003

Recall

Recall Number
Z-0036-04
Event Number
27242
Firm
VIASYS Med Systems
FEI Number
3011270181
Product Code
CAI
Status
Terminated
Root Cause
Other
Initiated
September 10, 2003
Posted
October 15, 2003
Terminated
March 24, 2004
Address
100 Chaddick Dr., Wheeling, IL, 60090

Description

Hyperinflation Circuit, consisting of a 2.0 L breathing bag, pressure monitoring tube, oxygen supply tubing, sideport connector with adjustable bleed valve and ported elbow; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83120

Reason

The exhalation hole in the sideport relief valve may be blocked, allowing excess pressure build-up.

Action

VIASYS telephoned the direct accounts and sent out follow-up faxes on 9/10-11/03, informing them of the potential for a blocked exhalation hole in the sideport relief valve cap which may result in excess pressure build-up. The accounts were instructed to check their inventory for the affected catalog numbers and lots numbers, place any found on hold for return to VIASYS, and sub-recall the affected product from their customers.

Distribution

Missouri, Texas, New York, Illinois, Kansas, California, Pennsylvania, Georgia, Arizona, Massachusetts, Maine, Oklahoma and Virginia.

Quantity

40 units