Z-1169-06

Syringe, 62RNR 2.5 Microliter Syringe, with needle point style 3 (blunt needle point for use with HPLC...

Name: Z-1169-06 Syringe, 62RNR 2.5 Microliter Syringe, with needle point style 3 (blunt needle point for use with HPLC...
Creator: Hamilton Co
Published: 2006-03-28
License: https://open.fda.gov/license/

Hamilton Co / initiated 2006-03-28 / Terminated

FDA source

Hamilton Co began a recall of Syringe, 62RNR 2.5 Microliter Syringe, with needle point style 3 (blunt needle point for use with HPLC injection valves and for sample pipetting) Part #: 87942 on 2006-03-28. The reason FDA records is "There is an error in the marking of the graduated divisions on syringes in affected lots that shows an amount that is double the actual volume of the syringe". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1169-06
Status: Terminated
Initiated: 2006-03-28
Posted: 2006-06-22
Terminated: 2006-12-21
Recalling firm: Hamilton Co
Product: Syringe, 62RNR 2.5 Microliter Syringe, with needle point style 3 (blunt needle point for use with HPLC injection valves and for sample pipetting) Part #: 87942.
Product code: JQW Station, Pipetting And Diluting, For Clinical Use
Reason for recall: There is an error in the marking of the graduated divisions on syringes in affected lots that shows an amount that is double the actual volume of the syringe
FDA root cause: Other
Action: On 3/28/06, the firm initiated the recall and its notification was via letters explaining the reason for the recall and requesting the product be returned.
Quantity in commerce: 63 units
Distribution: Worldwide-The product was distributed to 28 U.S. consignees and 3 foreign consignees. (Canada, Switzerland, Japan)
Product codes and lots: Lot 340007 and 342081

Product code JQW

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)