Hamilton Co Y-valve and T-valve, PSD/4 Syringe Drive Module parts. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Y-valve and T-valve, PSD/4 Syringe Drive Module parts.
Brand
Hamilton Co
Lot Codes / Batch Numbers
catalog number 7427-01 (Y-valve), catalog number 7990-01 (T-valve), catalog number 51863-01-IL (PSD/4 with valve and syringe), no 510k number. For 7427-01 (Lot number, date of manufacture): 277702, 4/29/2003, 282550A, 8/11/2003, 282550, 8/13/2003, 286630, 10/1/2003, 287449, 10/20/2003, 287137, 10/20/2003, 287949, 12/18/2003, 301809, 6/30/2004, 305599, 8/19/2005, 309328, 11/5/2004, 313276, 12/17/2004, 314662, 3/7/2005, 317940, 4/6/2005, 319506, 4/11/2005, 321121, 5/6/2005, 324204, 6/23/2005, 325483, 7/20/2005. For 7990-01: 277703, 4/30/2003, 283119, 9/30/2003 291279, 1/7/2004, 303942, 7/19/2004, 303687, 7/19/2004, 318833, 3/24/2005, 319684, 5/5/2005.
Products Sold
catalog number 7427-01 (Y-valve), catalog number 7990-01 (T-valve), catalog number 51863-01-IL (PSD/4 with valve and syringe), no 510k number. For 7427-01 (Lot number, date of manufacture): 277702, 4/29/2003; 282550A, 8/11/2003; 282550, 8/13/2003; 286630, 10/1/2003; 287449, 10/20/2003; 287137, 10/20/2003; 287949, 12/18/2003; 301809, 6/30/2004; 305599, 8/19/2005; 309328, 11/5/2004; 313276, 12/17/2004; 314662, 3/7/2005; 317940, 4/6/2005; 319506, 4/11/2005; 321121, 5/6/2005; 324204, 6/23/2005; 325483, 7/20/2005. For 7990-01: 277703, 4/30/2003; 283119, 9/30/2003 291279, 1/7/2004; 303942, 7/19/2004; 303687, 7/19/2004; 318833, 3/24/2005; 319684, 5/5/2005.
Hamilton Co is recalling Y-valve and T-valve, PSD/4 Syringe Drive Module parts. due to The product valve has a high probability of deforming and may result in leakage during use.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The product valve has a high probability of deforming and may result in leakage during use.
Recommended Action
Per FDA guidance
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).
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 noticeDistribution
As reported by FDA
CA, IN, MA, MI, WI
Page updated: Jan 10, 2026