FDA Medical Device Recalls (openFDA)
Interpore Cross International Inc: Spinal Implant, Catalog number: 1000-3000 through 1000-3015 (9 catalog numbers)
- Recall number
- Z-0530-05
- Recalling firm
- Interpore Cross International Inc
- Product
- Spinal Implant, Catalog number: 1000-3000 through 1000-3015 (9 catalog numbers)
- Status
- Terminated
- Initiated
- 2005-01-14
- Posted
- 2005-02-04
- Terminated
- 2005-03-03
- Reason
- Mislabeled.
- Root cause
- Other
- Action
- Firm sent recall letters on 1/18/2005 requesting return of product. A response form was enclosed.
- Quantity
- 63
- Distribution
- TN, MT, MI, CA, IN, PA, NJ, TX, KY, LA, CO.
- Lot, serial or model codes
- NEXUS Product List Of Catalog Numbers & Lot Numbers Catalog Number Lot Number/s 1000-3000 300510 303512A 302909A 303012 302812A 302912 302109 303009 1000-3001 326408A 304009 304509 1000-3003 301210 305809A 305509 304709A 305109 324508 1000-3004 304011A 310110 303911A 1000-3005 304211A 312410 301112 304311 1000-3010 302407 300404 1000-3011 313207 1000-3013 307404 312107 312307A 1000-3015 306911A 309505 305605 305905 307111
- 510(k) numbers
- ["K040168"]
- PMA numbers
- not on file
- Product code
- MQP
- 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