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Center for Biologics Evaluation: 39 warning letters

The full list. FDA warning letters from the Center for Biologics Evaluation and Research: 39 rows for $5, FDA warning letters issued November 12, 2024 to October 30, 2026. The list gains about 1 row a month. The new rows come each week by email, $19 a month.

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Updated October 13, 2026. Source: FDA warning letters (U.S. Food and Drug Administration).

FDA issued 39 warning letters from the Center for Biologics Evaluation and Research from December 12, 2024 to October 13, 2026, to 39 companies; 5 have a closeout letter. The newest, issued October 13, 2026 by the Center for Biologics Evaluation and Research, went to Calibrate IV Hydration (Unapproved New Drugs/Unlicensed Biological Product Violations).

The request: Every new FDA warning letter from the Center for Biologics Evaluation and Research, with the company, the subject and the letter.

SpecStream is the live web data engine for teams and agents. It reads FDA's warning letters table each morning, and this page is that reading. Ask for the offices, subjects or companies you follow and each new letter arrives in your sheet, CRM, Slack or agent as FDA posts it.

  • 39Letters
  • 5With closeout
  • October 13, 2026Latest issued

Newest letters

The newest 39 of 39 by issue date, each linked to the letter on fda.gov.

IssuedCompanyIssuing officeSubjectPostedSource
October 13, 2026Calibrate IV HydrationCenter for Biologics Evaluation and ResearchUnapproved New Drugs/Unlicensed Biological Product ViolationsOctober 27, 2026fda.gov
October 6, 2026Tides Medical LLCCenter for Biologics Evaluation and ResearchInvestigational Device Exemptions (IDE)/Premarket Approval Application (PMA)October 20, 2026fda.gov
September 25, 2026Beaute BountyCenter for Biologics Evaluation and ResearchUnapproved New Drugs/Unlicensed Biological Product ViolationsOctober 27, 2026fda.gov
September 11, 2026NexCell Scientific IncCenter for Biologics Evaluation and ResearchUnapproved New Drugs/Unlicensed Biological Product ViolationsSeptember 22, 2026fda.gov
August 27, 2026Stephen J. Fallon, Ph.D.Center for Biologics Evaluation and ResearchBioresearch Monitoring Program/Institutional Review Board (IRB)September 8, 2026fda.gov
August 14, 2026R3 Medical CompaniesCenter for Biologics Evaluation and ResearchUnapproved New Drugs/Unlicensed Biological Product ViolationsAugust 25, 2026fda.gov
June 22, 2026Genzyme Ireland LimitedCenter for Biologics Evaluation and ResearchCGMP/Deviations/Biologics License Application (BLA)June 30, 2026fda.gov
May 26, 2026Blue Horizon International, LLCCenter for Biologics Evaluation and ResearchUnapproved New Drugs/Unlicensed Biological Product ViolationsJune 2, 2026fda.gov
April 22, 2026Estar Technologies LtdCenter for Biologics Evaluation and ResearchInvestigational Device Exemptions (IDE)/Premarket Approval Application (PMA) Adulterated DeviceMay 12, 2026fda.gov
March 17, 20264U HealthCenter for Biologics Evaluation and ResearchPremarket Approval/AdulteratedMarch 24, 2026fda.gov
February 11, 2026Dynamic Stem Cell TherapyCenter for Biologics Evaluation and ResearchUnapproved New Drugs/Unlicensed Biological Product ViolationsFebruary 24, 2026fda.gov
February 10, 2026ProDx HealthCenter for Biologics Evaluation and ResearchInvestigational Device Exemptions (IDE)/Premarket Approval Application (PMA)February 10, 2026fda.gov
January 29, 2026Central Coast Multispecialty Medical Group, Inc.Center for Biologics Evaluation and ResearchDeviations/CFR/Regulations for Human Cells, Tissues & Cellular Products (HCT/Ps)February 10, 2026fda.gov
January 27, 2026Conceive Fertility CenterCenter for Biologics Evaluation and ResearchDeviations/CFR/Regulations for Human Cells, Tissues & Cellular Products (HCT/Ps)February 10, 2026fda.gov
January 23, 2026Louisville Reproductive CenterCenter for Biologics Evaluation and ResearchDeviations/CFR/Regulations for Human Cells, Tissues & Cellular Products (HCT/Ps)February 10, 2026fda.gov
January 9, 2026GermaphobixCenter for Biologics Evaluation and ResearchInvestigational Device Exemptions (IDE)/Premarket Approval Application (PMA)January 20, 2026fda.gov
January 8, 2026GenovateCenter for Biologics Evaluation and ResearchInvestigational Device Exemptions (IDE)/Premarket Approval Application (PMA)January 20, 2026fda.gov
January 8, 2026GenetraceCenter for Biologics Evaluation and ResearchInvestigational Device Exemptions (IDE)/Premarket Approval Application (PMA)January 20, 2026fda.gov
December 3, 2025Microvascular Tissue, Inc.Center for Biologics Evaluation and ResearchCGMP/Deviations/Biologics License Application (BLA)December 16, 2025fda.gov
December 3, 2025Green Valley Fertility PartnersCenter for Biologics Evaluation and ResearchDeviations/CFR/Regulations for Human Cells, Tissues & Cellular Products (HCT/Ps)December 16, 2025fda.gov
September 30, 2025Allovate Therapeutics, LLCCenter for Biologics Evaluation and ResearchCGMP/Deviations/Biologics License Application (BLA)October 14, 2025fda.gov
September 24, 2025New Life Medical Services, LLCCenter for Biologics Evaluation and ResearchCGMP/Deviations/Biologics License Application (BLA)October 7, 2025fda.gov
September 12, 2025Cellebration LLCCenter for Biologics Evaluation and ResearchDeviations/CFR/Regulations for Human Cells, Tissues & Cellular Products (HCT/Ps)September 23, 2025fda.gov
September 9, 2025CSL BehringCenter for Biologics Evaluation and ResearchAdvertising & Promotional Labeling/Drugs/Biological ProductsSeptember 16, 2025fda.gov
September 4, 2025NuVida Medical LLCCenter for Biologics Evaluation and ResearchDeviations/CFR/Regulations for Human Cells, Tissues & Cellular Products (HCT/Ps)September 16, 2025fda.gov
August 15, 2025Platinum Biologics LLCCenter for Biologics Evaluation and ResearchDeviations/CFR/Regulations for Human Cells, Tissues & Cellular Products (HCT/Ps)August 26, 2025fda.gov
August 15, 2025Innate Healthcare InstituteCenter for Biologics Evaluation and ResearchDeviations/CFR/Regulations for Human Cells, Tissues & Cellular Products (HCT/Ps)August 26, 2025fda.gov
July 7, 2025O3UV, LLCCenter for Biologics Evaluation and ResearchInvestigational Device Exemptions (IDE)/Premarket Approval Application (PMA) Adulterated DeviceJuly 22, 2025fda.gov
June 13, 2025InVia Fertility Specialists, PLLCCenter for Biologics Evaluation and ResearchDeviations/CFR/Regulations for Human Cells, Tissues & Cellular Products (HCT/Ps)July 1, 2025fda.gov
May 5, 2025Supreme Rejuvenation, LLCCenter for Biologics Evaluation and ResearchUnapproved New Drugs/MisbrandedMay 20, 2025fda.gov
March 25, 2025Amy Lightner, MDCenter for Biologics Evaluation and ResearchBioresearch Monitoring ProgramJune 3, 2025fda.gov
March 10, 2025MG InfusionsCenter for Biologics Evaluation and ResearchCGMP/Deviations/Biologics License Application (BLA)March 18, 2025fda.gov
February 14, 2025Sperm Bank, Inc. dba Fertility Center of CaliforniaCenter for Biologics Evaluation and ResearchDeviations/CFR/Regulations for Human Cells, Tissues & Cellular Products (HCT/Ps)February 25, 2025fda.gov
January 17, 2025BioStem Life SciencesCenter for Biologics Evaluation and ResearchDeviations/CFR/Regulations for Human Cells, Tissues & Cellular Products (HCT/Ps)February 4, 2025fda.gov
January 17, 2025Chara Biologics, Inc.Center for Biologics Evaluation and ResearchCGMP/Deviations/Biologics License Application (BLA)January 28, 2025fda.gov
December 30, 2024Evolutionary Biologics Inc.Center for Biologics Evaluation and ResearchDeviations/CFR/Regulations for Human Cells, Tissues & Cellular Products (HCT/Ps)January 28, 2025fda.gov
December 16, 2024Skye Biologics Holdings LLCCenter for Biologics Evaluation and ResearchDeviations/CFR/Regulations for Human Cells, Tissues & Cellular Products (HCT/Ps)May 20, 2025fda.gov
December 12, 2024INCELL Corporation LLCCenter for Biologics Evaluation and ResearchCGMP/Finished Pharmaceuticals/Unapproved New Drug/Misbranded/AdulteratedJanuary 21, 2025fda.gov
December 12, 2024XO Biologix, LLCCenter for Biologics Evaluation and ResearchUnapproved New Drugs/AdulteratedJanuary 7, 2025fda.gov

By subject group

Subject groupLettersLatest
Biologics, cells and tissue26October 13, 2026
Medical devices7October 6, 2026
Other subjects2March 17, 2026
Unapproved drugs, marketing and online sales2May 5, 2025
Clinical research and labs1August 27, 2026
Drug manufacturing (CGMP)1December 12, 2024

By year issued

YearLettersLatest
202618October 13, 2026
202517December 3, 2025
20244December 30, 2024

Where FDA publishes its warning letters

Public domain (U.S. government work). Letters are as FDA lists them in its warning letters table: the company, the issue and posting dates, the issuing office and FDA's subject line. Subject groups are SpecStream's, read from the words of that subject line. FDA posts a letter some weeks after it issues it, so the newest weeks fill in later. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.

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