Y-valve and T-valve, PSD/4 Syringe Drive Module parts.
FDA device recall Z-0087-06 · posted 2005-10-22 · Terminated
Recall details
- Recalling firm
- Hamilton Co
- Reason for recall
- The product valve has a high probability of deforming and may result in leakage during use.
- Action taken
- 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
- Status
- Terminated
- Product code
- JJC
- Quantity affected
- 271 Y and 78 T valves were distributed.
- Distribution
- One distributor and 8 consumers received this product in CA, MA, MI, WI, Japan and Switzerland.
- Date initiated
- 2005-08-24
- Date posted
- 2005-10-22
- Date terminated
- 2006-03-24
- Location
- Reno, NV
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