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LifeSouth Community Blood Centers, Inc. FDA Inspection Record

FEI 1038804 · Inspections, Form 483s, warning letters and import refusals

LifeSouth Community Blood Centers, Inc. is an FDA-inspected facility (FEI 1038804) located in Brooksville, FL, US. RegDataLab tracks 7 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Feb 24, 2026: No Action Indicated (NAI)
Inspections on record
7 (7 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
Recalls as the recalling firm
12, latest Dec 27, 2022

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Feb 24, 2026No Action Indicated (NAI)No citations listed
Dec 8, 2021No Action Indicated (NAI)No citations listed
May 7, 2018No Action Indicated (NAI)No citations listed
May 11, 2016No Action Indicated (NAI)No citations listed
Jul 15, 2014No Action Indicated (NAI)No citations listed
Jul 26, 2012No Action Indicated (NAI)No citations listed
Jun 10, 2010No Action Indicated (NAI)No citations listed

Recalls

Showing the 10 most recent of 12 recalls. Recalls FDA's Enforcement Report lists with this FEI as the recalling firm. The recalling firm is not always the site that made the product. Search FDA's Enforcement Report by recall number.

DateClassRecallProduct and reason
Dec 27, 2022Class IIB-0299-2023Apheresis Platelets, Leukocytes Reduced
Platelet product, in which platelet yield did not meet specifications, was distributed.
Jan 26, 2017Class IIB-0431-2017Apheresis Platelets, Leukocytes Reduced
Plateletpheresis products, lacking proper quality control testing, were distributed.
Oct 24, 2008Class IIB-1046-13Platelets Pheresis Leukocytes Reduced
Blood product, with a low platelet count, was distributed.
Oct 24, 2008Class IIB-1047-13Platelets Pheresis Leukocytes Reduced
Blood product, with a low platelet count, was distributed.
Sep 25, 2008Class IIB-0091-14Platelets Pheresis Leukocytes Reduced
Blood product, which did not meet acceptable product specifications, was distributed.
Aug 13, 2008Class IIB-1164-13Platelets Pheresis Leukocytes Reduced
Blood product, with a low platelet count, was distributed.
Jun 14, 2007Class IIB-0944-08Platelets Pheresis Leukocytes Reduced
Blood product, with a low platelet count, was distributed.
Mar 9, 2007Class IIB-0924-13Fresh Frozen Plasma (Apheresis)
Blood products, collected in a manner that may have compromised the sterility of the collection system, were distributed.
Apr 29, 2006Class IIB-0223-7Red Blood Cells
Blood products, which were collected from a donor who had traveled to a malarial endemic area, were distributed.
Apr 21, 2006Class IIB-0185-7Platelets Pheresis Leukocytes Reduced
Blood product, which did not meet acceptable product specifications, was distributed.

FDA record score

3 of 100. A count of this site's adverse public FDA records, weighted by how recent each one is. A higher number means more, or more recent, records. Each record below adds the points shown.

Counted on Nov 15, 2026, method version 1. It counts records and does not judge the site: a low number does not establish that a site is safe, and sites that FDA inspects more often can collect more points. How this is counted.

12 records behind this number
RecordDatePoints x age weightAdds
Class II recall B-0299-2023, this FEI as the recalling firmDec 27, 20224 x 0.62.4
Class II recall B-0431-2017, this FEI as the recalling firmJan 26, 20174 x 0.251
Class II recall B-1046-13, this FEI as the recalling firmOct 24, 200810 years or older, so it adds no points0
Class II recall B-1047-13, this FEI as the recalling firmOct 24, 200810 years or older, so it adds no points0
Class II recall B-0091-14, this FEI as the recalling firmSep 25, 200810 years or older, so it adds no points0
Class II recall B-1164-13, this FEI as the recalling firmAug 13, 200810 years or older, so it adds no points0
Class II recall B-0944-08, this FEI as the recalling firmJun 14, 200710 years or older, so it adds no points0
Class II recall B-0924-13, this FEI as the recalling firmMar 9, 200710 years or older, so it adds no points0
Class II recall B-0223-7, this FEI as the recalling firmApr 29, 200610 years or older, so it adds no points0
Class II recall B-0185-7, this FEI as the recalling firmApr 21, 200610 years or older, so it adds no points0
Class II recall B-0222-7, this FEI as the recalling firmMar 10, 200610 years or older, so it adds no points0
Class II recall B-0439-7, this FEI as the recalling firmOct 14, 200510 years or older, so it adds no points0

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 14, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 14, 2026Newest record Nov 5, 2026Current
Compliance actions (warning letters, injunctions and other action types)Nov 2, 2026Newest record Oct 29, 2026Current
Warning letter textNov 14, 2026Newest record Nov 10, 2026Current
Recalls (Enforcement Report)Nov 14, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 2, 2026Newest record Oct 22, 2026Current

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Facility details

Company
LifeSouth Community Blood Centers, Inc.
Location
Brooksville, FL (US)
Source
inspections

FDA data resources

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