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Carter BloodCare

FDA Regulatory Profile

Carter BloodCare has 0 FDA recalls, 45 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 21, 2026 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections45Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 21, 2026Plano, TXBiologicsNo Action Indicated (NAI)1000143652
Jun 24, 2026Flower Mound, TXBiologicsNo Action Indicated (NAI)3000717800
Jun 5, 2025Mckinney, TXBiologicsNo Action Indicated (NAI)3022204129
Dec 17, 2024Mansfield, TXBiologicsNo Action Indicated (NAI)3005680006
Dec 4, 2024Rockwall, TXBiologicsNo Action Indicated (NAI)3000204655
Jun 27, 2024Frisco, TXBiologicsNo Action Indicated (NAI)3012540622
Jan 11, 2024Woodway, TXBiologicsNo Action Indicated (NAI)3003830999
Aug 22, 2023Bedford, TXBiologicsNo Action Indicated (NAI)3002603147
Jun 14, 2023Rockwall, TXBiologicsNo Action Indicated (NAI)3000204655
Feb 14, 2020Mansfield, TXBiologicsNo Action Indicated (NAI)3005680006
Aug 9, 2019Flower Mound, TXBiologicsNo Action Indicated (NAI)3000717800
May 23, 2019Plano, TXBiologicsNo Action Indicated (NAI)1000143652
Apr 12, 2019Bedford, TXBiologicsNo Action Indicated (NAI)3002603147
Apr 5, 2019Woodway, TXBiologicsNo Action Indicated (NAI)3003830999
Oct 26, 2018Frisco, TXBiologicsVoluntary Action Indicated (VAI)3012540622
Aug 15, 2018Rockwall, TXBiologicsNo Action Indicated (NAI)3000204655
Dec 6, 2017Bedford, TXBiologicsVoluntary Action Indicated (VAI)3002603147
Oct 5, 2017Mansfield, TXBiologicsNo Action Indicated (NAI)3005680006
Aug 25, 2017Plano, TXBiologicsNo Action Indicated (NAI)1000143652
Aug 2, 2017Woodway, TXBiologicsNo Action Indicated (NAI)3003830999

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 1000143652Plano, TX6Jul 21, 2026
FEI 3000717800Flower Mound, TX7Jun 24, 2026
FEI 3022204129Mckinney, TX1Jun 5, 2025
FEI 3005680006Mansfield, TX7Dec 17, 2024
FEI 3000204655Rockwall, TX7Dec 4, 2024
FEI 3012540622Frisco, TX2Jun 27, 2024
FEI 3003830999Woodway, TX6Jan 11, 2024
FEI 3002603147Bedford, TX6Aug 22, 2023
FEI 1640700Mount Pleasant, TX3Jun 11, 2014

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.