FDA Medical Device Recalls (openFDA)
Tecan U S Inc: Disposable Tips 1000 l with filter Conductive disposable tips for Tecan Genesis Series * Order Number 612513.1 * Tecan Schweiz AG Seestrae 103, CH-8708 Mannedorf, Switzerland * Made in Germany. Blister 1 x 96 pcs.
- Recall number
- Z-0326-06
- Recalling firm
- Tecan U S Inc
- Product
- Disposable Tips 1000 l with filter Conductive disposable tips for Tecan Genesis Series * Order Number 612513.1 * Tecan Schweiz AG Seestrae 103, CH-8708 Mannedorf, Switzerland * Made in Germany. Blister 1 x 96 pcs.
- Status
- Terminated
- Initiated
- 2005-04-11
- Posted
- 2005-12-23
- Terminated
- 2006-05-18
- Reason
- Double filtering of 1000 l tips. The defect could result in cross contamination of other samples due to possible dripping of sample while moving over other samples.
- Root cause
- Other
- Action
- The consignee was notified via fax''d letter on/about 11/08/2005.
- Quantity
- 3000 Tips
- Distribution
- IL and Europe
- Lot, serial or model codes
- Part Number 10612523, Lot No. U122098L-1325, Lot No. U122098L-3225 & Lot No. U122098L-2325. The sub-lot numbers (i.e. 1325, 3225 and 2325) are printed on each blister and stamped in blue colour on the shipping container in the upper right corner of the box.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- JQW
- Firm FEI
- 1037985
- Firm city
- Research Triangle Park
- Firm state
- NC
- 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