FDA Medical Device Recalls (openFDA)
Humagen Fertility Diagnostics, Inc.: IVF Pasteur Pipettes, glass, cotton plugged, length 9", in boxes of 90 consisting of 30 nylon tube packages of 3 pipettes each. Item # PP-9-90PL. Boxes are labeled in part ***Humagen Fertility Diagnostics, Inc. 2400 Hunter's Way Charlottesville, VA 22911***
- Recall number
- Z-1220-2007
- Recalling firm
- Humagen Fertility Diagnostics, Inc.
- Product
- IVF Pasteur Pipettes, glass, cotton plugged, length 9", in boxes of 90 consisting of 30 nylon tube packages of 3 pipettes each. Item # PP-9-90PL. Boxes are labeled in part ***Humagen Fertility Diagnostics, Inc. 2400 Hunter's Way Charlottesville, VA 22911***
- Status
- Terminated
- Initiated
- 2007-05-08
- Posted
- 2007-09-18
- Terminated
- 2007-10-29
- Reason
- Pasteur pipettes for laboratory use were labeled as sterile but may have become contaminated.
- Root cause
- Other
- Action
- The recalling firm notified consignees by phone and e-mail on 05/07/07. International consignees were advised to discard product for replacement.
- Quantity
- 160 boxes
- Distribution
- The recalled product was distributed to 2 direct accounts in IL and to 6 international distributors in United Kingdom, Greece, Australia, United Arab Emirates, the Netherlands, and Israel.
- Lot, serial or model codes
- 160306022 EXP 1/22/2010 160306046 EXP 2/15/2010 160306065 EXP 3/6/2010
- 510(k) numbers
- ["K000915"]
- PMA numbers
- not on file
- Product code
- MQK
- Firm FEI
- 1216677
- Firm city
- Charlottesville
- Firm state
- VA
- 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