Z-0087-06

Y-valve and T-valve, PSD/4 Syringe Drive Module parts

Name: Z-0087-06 Y-valve and T-valve, PSD/4 Syringe Drive Module parts
Creator: Hamilton Co
Published: 2005-08-24
License: https://open.fda.gov/license/

Hamilton Co / initiated 2005-08-24 / Terminated

FDA source

Hamilton Co began a recall of Y-valve and T-valve, PSD/4 Syringe Drive Module parts on 2005-08-24. The reason FDA records is "The product valve has a high probability of deforming and may result in leakage during use". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0087-06
Status: Terminated
Initiated: 2005-08-24
Posted: 2005-10-22
Terminated: 2006-03-24
Recalling firm: Hamilton Co
Product: Y-valve and T-valve, PSD/4 Syringe Drive Module parts.
Product code: JJC Analyzer, Chemistry (Sequential Multiple, Continuous Flow) Clinical Use
Reason for recall: The product valve has a high probability of deforming and may result in leakage during use.
FDA root cause: Other
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).
Quantity in commerce: 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.
Product codes and lots: 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.

Product code JJC

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)