Interpore Cross International Inc Spinal Implant, Catalog number: 1000-3000 through 1000-3015 (9 catalog numbers) Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Spinal Implant, Catalog number: 1000-3000 through 1000-3015 (9 catalog numbers)
Brand
Interpore Cross International Inc
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
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
Interpore Cross International Inc is recalling Spinal Implant, Catalog number: 1000-3000 through 1000-3015 (9 catalog numbers) due to Mislabeled.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Mislabeled.
Recommended Action
Per FDA guidance
Firm sent recall letters on 1/18/2005 requesting return of product. A response form was enclosed.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, CO, IN, KY, LA, MI, MT, NJ, PA, TN, TX
Page updated: Jan 10, 2026