FDA Medical Device Recalls (openFDA)
Hamilton Co: Hamilton brand Disposable Precision Tips, Part Number 235300 (box containing 504 tips) and 235400 (case containing 20 boxes), Manufactured by Hamilton Company, Reno, Nevada
- Recall number
- Z-0723-2007
- 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
- Status
- Terminated
- Initiated
- 2007-01-30
- Posted
- 2007-04-07
- Terminated
- 2007-11-28
- Reason
- 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
- 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
- 37 cases
- Distribution
- Nationwide (via a single distributor in New Jersey)
- Lot, serial or model codes
- Lot: 33906 P5 and Lot: 63906 P5
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- -JTC
- Firm FEI
- 2915796
- Firm city
- Reno
- Firm state
- NV
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28