100 inch (254 cm) 15 Drop Administration Set with FlowSafe Flow Controller and Max Y Connector, 50 per box. Product No. MFS102
FDA Recall Z-0152-04 · Posted 2004-07-20
Recalling FirmMaximus Medical Products Inc
Recall StatusTerminated
Product CodeFPA
Date Initiated2003-10-30
Date Terminated2003-11-25
Product Quantity63 cases, 50 per case.
Reason for Recall
Mislabeled with wrong drop size drip chamber specification.
Firm Action
The firm called and sent fax recall letters on or about 10/30/2003. Labels were shipped and applied to stock in question. Recall is complete.
Root Cause
Other
Distribution Pattern
CO, PA,
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.