Y-valve and T-valve, PSD/4 Syringe Drive Module parts.
FDA Recall Z-0087-06 · Posted 2005-10-22
Recalling FirmHamilton Co
Recall StatusTerminated
Product CodeJJC
Date Initiated2005-08-24
Date Terminated2006-03-24
Product Quantity271 Y and 78 T valves were distributed.
Reason for Recall
The product valve has a high probability of deforming and may result in leakage during use.
Firm Action
Recall initiated on 08/24/2005. The firm issued notification to its consignees via overnight letter, and via e-mail for its distributor (Hamilton Bonaduz).
Root Cause
Other
Distribution Pattern
One distributor and 8 consumers received this product in CA, MA, MI, WI, Japan and Switzerland.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.