BD Vacutainer CPT Cell Preparation Tube with Sodium CitrateRecalls & reported problems across all models

We found 2 models of BD Vacutainer CPT Cell Preparation Tube with Sodium Citrate by Becton, Dickinson And Company in the FDA's device registry (GUDID). Together they are named in 415 adverse event reports in the FDA's MAUDE database, received between Oct 17, 2017 and Jul 29, 2026 — classified as 1 injury, 414 malfunctions.

The most frequently reported specific device problem is “Incorrect, Inadequate or Imprecise Result or Readings” (130 reports).

1 FDA recall record name at least one of these models by its device identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

BD Vacutainer CPT Cell Preparation Tube with Sodium Citrate recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. May 25, 2022Class IIOpen, Classified

   Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

   Z-1618-2022 · Root cause: Environmental control · Recall details · FDA record ↗

Most reported BD Vacutainer CPT Cell Preparation Tube with Sodium Citrate problems

BD Vacutainer CPT Cell Preparation Tube with Sodium Citrate models

2 models, most reported first. Each model has its own page with its reports, recalls and device details.

• BD Vacutainer® CPT™ Cell Preparation Tube with Sodium Citrate 362761

  LYMPHOCYTE SEPARATION MEDIUM
  1 recall286 reports
• BD Vacutainer® CPT™ Cell Preparation Tube with Sodium Citrate 362760

  LYMPHOCYTE SEPARATION MEDIUM
  129 reports

Recent BD Vacutainer CPT Cell Preparation Tube with Sodium Citrate adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

• MalfunctionJul 29, 2026Incorrect, Inadequate or Imprecise Result or Readings

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50072928 ↗
• MalfunctionJul 27, 2026Short Fill; Improper Chemical Reaction

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50020589 ↗
• MalfunctionApr 22, 2026Short Fill

  IT WAS REPORTED WHILE USING BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE, ONE TUBE UNDERFILLED. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24954300 ↗
• MalfunctionFeb 19, 2026Device Ingredient or Reagent Problem

  IT WAS REPORTED AFTER USING BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE, THERE WAS POOR BARRIER SEPARATION SEEN IN AN UNSPECIFIED NUMBER OF TUBES. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24396940 ↗
• MalfunctionFeb 2, 2026Device Ingredient or Reagent Problem

  IT WAS REPORTED WHILE USING BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE, AN UNSPECIFIED NUMBER OF TUBES EXHIBITED POOR BARRIER SEPARATION AFTER PROCESSING. THERE WAS NO HEALTH IMPACT OR CONSEQUENCES REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24239969 ↗
• MalfunctionJan 30, 2026Short Fill

  IT WAS REPORTED WHILE USING BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE, ONE (1) OF TUBE UNDERFILLED. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24228424 ↗
• MalfunctionJan 21, 2026Device Ingredient or Reagent Problem

  IT WAS REPORTED WHILE USING BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE, AN UNSPECIFIED NUMBER OF TUBES EXHIBITED POOR BARRIER SEPARATION. THERE WAS NO HEALTH IMPACT OR CONSEQUENCES REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24139369 ↗
• MalfunctionDec 17, 2025Short Fill; Short Fill

  IT WAS REPORTED WHILE USING BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE, AN UNSPECIFIED NUMBER OF TUBES HAD VACUUM LOSS RESULTING IN UNDERFILLED TUBES. THE TUBES WERE REPLACED. THERE WAS NO HEALTH IMPACT OR CONSEQUENCES REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23835405 ↗
• MalfunctionDec 3, 2025Device Ingredient or Reagent Problem; Device Ingredient or Reagent Problem

  IT WAS REPORTED WHILE USING BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE, AN UNSPECIFIED NUMBER OF TUBES EXHIBITED POOR BARRIER SEPARATION (BLOOD IS NOT PASSING THROUGH FICOLL LAYER). THERE WAS NO HEALTH IMPACT OR CONSEQUENCES REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23711545 ↗
• MalfunctionNov 20, 2025Improper Chemical Reaction; Improper Chemical Reaction

  IT WAS REPORTED THAT WHILE USING BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE AN UNSPECIFIED NUMBER OF TUBES EXHIBITED POOR BARRIER SEPARATION. THERE WAS NO HEALTH IMPACT OR CONSEQUENCES REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23609558 ↗
• MalfunctionNov 19, 2025Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material

  IT WAS REPORTED PRIOR TO USING BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE, AN UNSPECIFIED NUMBER OF TUBES EXHIBITED A STRING-LIKE MATTER IN THE LIQUID DENSITY MEDIA (LDM). THERE WAS NO HEALTH IMPACT OR CONSEQUENCES REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23599666 ↗
• MalfunctionOct 22, 2025Device Ingredient or Reagent Problem; Device Ingredient or Reagent Problem

  REPORT 1 OF 2: IT WAS REPORTED WHILE USING BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE, 1 SAMPLE EXHIBITED POOR BARRIER CENTRIFUGATION. THERE WAS NO HEALTH IMPACT OR CONSEQUENCES REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23359175 ↗
• MalfunctionOct 22, 2025Device Ingredient or Reagent Problem; Device Ingredient or Reagent Problem

  REPORT 2 OF 2: IT WAS REPORTED WHILE USING BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE, AN UNSPECIFIED NUMBER OF SAMPLES EXHIBITED POOR BARRIER CENTRIFUGATION. THERE WAS NO HEALTH IMPACT OR CONSEQUENCES REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23358999 ↗
• MalfunctionOct 22, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem

  IT WAS REPORTED PRIOR TO USE OF 21 CASES OF BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE, THE OUTER CASE HAD AN INCORRECT EXPIRATION DATE. THERE WAS NO HEALTH IMPACT OR CONSEQUENCES REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23357688 ↗
• MalfunctionOct 16, 2025Device Ingredient or Reagent Problem; Device Ingredient or Reagent Problem

  IT WAS REPORTED THAT WHEN USING THE BD VACUTAINER® CPT¿ CELL PREPARATION TUBE WITH SODIUM CITRATE, AN UNSPECIFIED NUMBER OF TUBES EXHIBITED POOR BARRIER SEPARATION. NO ADVERSE IMPACT WAS REPORTED REGARDING THE PATIENT OR USER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23311101 ↗

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