LifeShare Blood Center

FDA Regulatory Profile

LifeShare Blood Center has 0 FDA recalls, 32 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
May 18, 2026 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections32Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 18, 2026Shreveport, LABiologicsNo Action Indicated (NAI)3032139209
Aug 21, 2025Shreveport, LABiologicsNo Action Indicated (NAI)2370879
Oct 30, 2024Texarkana, TXBiologicsNo Action Indicated (NAI)3015186012
Jul 12, 2024Lafayette, LABiologicsNo Action Indicated (NAI)3022728367
Feb 9, 2024Beaumont, TXBiologicsNo Action Indicated (NAI)1672230
Aug 31, 2023Shreveport, LABiologicsNo Action Indicated (NAI)2370879
Mar 10, 2023Bossier City, LABiologicsNo Action Indicated (NAI)3001632629
Sep 14, 2022Alexandria, LABiologicsNo Action Indicated (NAI)2377718
Sep 1, 2022Lafayette, LABiologicsNo Action Indicated (NAI)3022728367
Apr 25, 2022El Dorado, ARBiologicsNo Action Indicated (NAI)3016665637
Feb 25, 2022Beaumont, TXBiologicsNo Action Indicated (NAI)1672230
Nov 19, 2019Bossier City, LABiologicsVoluntary Action Indicated (VAI)3001632629
Aug 9, 2019Shreveport, LABiologicsVoluntary Action Indicated (VAI)2370879
Jun 26, 2019Texarkana, TXBiologicsNo Action Indicated (NAI)3015186012
Dec 13, 2018Alexandria, LABiologicsNo Action Indicated (NAI)2377718
May 24, 2018Beaumont, TXBiologicsNo Action Indicated (NAI)1672230
Jul 26, 2017Bossier City, LABiologicsNo Action Indicated (NAI)3001632629
May 25, 2017Alexandria, LABiologicsVoluntary Action Indicated (VAI)2377718
May 23, 2017Shreveport, LABiologicsNo Action Indicated (NAI)2370879
Sep 13, 2016Beaumont, TXBiologicsNo Action Indicated (NAI)1672230

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 3032139209Shreveport, LA1May 18, 2026
FEI 2370879Shreveport, LA7Aug 21, 2025
FEI 3015186012Texarkana, TX2Oct 30, 2024
FEI 3022728367Lafayette, LA2Jul 12, 2024
FEI 1672230Beaumont, TX7Feb 9, 2024
FEI 3001632629Bossier City, LA6Mar 10, 2023
FEI 2377718Alexandria, LA6Sep 14, 2022
FEI 3016665637El Dorado, AR1Apr 25, 2022

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