FDA Medical Device Recalls (openFDA)
Interpore Cross International Inc: TPS-TL Straight Drill Guide Applicator, Catalog Number 1300-9016.
- Recall number
- Z-0659-03
- Recalling firm
- Interpore Cross International Inc
- Product
- TPS-TL Straight Drill Guide Applicator, Catalog Number 1300-9016.
- Status
- Terminated
- Initiated
- 2003-02-07
- Posted
- 2003-03-20
- Terminated
- 2003-08-28
- Reason
- Instrument fell apart during cleaning prior to surgery.
- Root cause
- Other
- Action
- Firm telephoned customers on 2/7/2003 requesting that they immediately return thier instruments.
- Quantity
- 37 units
- Distribution
- States of NJ, CA, PA, MN, WI, MO, FL, OH, VA, MD, Wash DC, NY, CO, MA and to Brazil, Mexico, England, Denmark, Belgium, Australia.
- Lot, serial or model codes
- Lot 32688
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LXH
- Firm FEI
- 1000160576
- Firm city
- Irvine
- Firm state
- CA
- 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