Z-0723-2007

Hamilton brand Disposable Precision Tips, Part Number 235300 (box containing 504 tips) and 235400 (case...

Name: Z-0723-2007 Hamilton brand Disposable Precision Tips, Part Number 235300 (box containing 504 tips) and 235400 (case...
Creator: Hamilton Co
Published: 2007-01-30
License: https://open.fda.gov/license/

Hamilton Co / initiated 2007-01-30 / Terminated / root cause: packaging

FDA source

Hamilton Co began a recall of Hamilton brand Disposable Precision Tips, Part Number 235300 (box containing 504 tips) and 235400 (case containing 20 boxes), Manufactured by Hamilton Company... on 2007-01-30. The reason FDA records is "Some of the packaged tips have increased force during aspiration, which can lead to pipetting errors such as LLD error messages, and also has risk of causing a missed pipetting". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as packaging.

Recall record

Recall number: Z-0723-2007
Status: Terminated
Initiated: 2007-01-30
Posted: 2007-04-07
Terminated: 2007-11-28
Recalling firm: Hamilton Co
Product: Hamilton brand Disposable Precision Tips, Part Number 235300 (box containing 504 tips) and 235400 (case containing 20 boxes), Manufactured by Hamilton Company, Reno, Nevada
Product code: -JTC
Reason for recall: Some of the packaged tips have increased force during aspiration, which can lead to pipetting errors such as LLD error messages, and also has risk of causing a missed pipetting.
Root cause tag: packaging
FDA root cause: Other
Action: The firm initiated its recall on January 30, 2007. The initial notification was sent via certified mail and e-mail. Subrecalls will be conducted by the distributor.
Quantity in commerce: 37 cases
Distribution: Nationwide (via a single distributor in New Jersey)
Product codes and lots: Lot: 33906 P5 and Lot: 63906 P5

Product code -JTC

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)