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BD PrepMate™ Consumables Kit 491455Recalls & reported problems

Becton, Dickinson And Company · Kit Prepmate Consume 480 Test · Class 3

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00382904914554), received between Oct 13, 2021 and Oct 13, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Markings/Labelling Problem” (1 report).

11 other recalls cover devices cleared under the same FDA submission (P970018); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Device Markings/Labelling Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionOct 13, 2021Device Markings/Labelling Problem; Device Markings/Labelling Problem

    IT WAS REPORTED THAT WHILE USING KIT PREPMATE CONSUME 480 TEST MISSING LABEL INFORMATION WAS OBSERVED BY THE LABORATORY PERSONNEL. THERE WAS NO REPORT OF PATIENT IMPACT. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: " FAILURE IN ONE OF THE KIT COMPONENTS (CENTRIFUGE TUBES SPARE PART #500024398) AND ILLEGIBLE PACKAGE BATCH".

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12628646 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P970018. One submission often covers many models, so check the product and lot details in each record.

  • Z-0877-2017 · Feb 12, 2016 · Terminated
    BD SurePathTM Preservative Collection Vials, catalog numbers 490505, 490527, 491095, 491096, and 491097. SurePath Preservative Fluid is designed for use with the PrepStain System
  • Z-1811-2012 · Mar 22, 2012 · Terminated
    PrepStain Syringing Pipettes 240 (Catalog #490517)
  • Z-1812-2012 · Mar 22, 2012 · Terminated
    PrepStain GYN 480 Disposable Test Kit with PreCoat Slides (Catalog #490523
  • Z-1814-2012 · Mar 22, 2012 · Terminated
    Manual Method 1: 480 Test Kit (PreCoat), Catalog/Model # 490529
  • Z-1813-2012 · Mar 22, 2012 · Terminated
    PrepStain Installation Kit (PreCoat), Catalog/Model # 490528
  • Z-1815-2012 · Mar 22, 2012 · Terminated
    PrepStain GN 480 Disposable Kit Catalog/Model 490542 This is a complete kit, per the firm's explanation, that contains the PrepStain Syringing Pipettes 240, the product being recal
  • Z-2087-2012 · Dec 8, 2011 · Terminated
    PrepStain Slide Processor. The PrepStain System is a liquid-based thin layer cell preparation process. The PrepStain System produces SurePath Slides that are intended for use in t
  • Z-2086-2012 · Dec 8, 2011 · Terminated
    PrepStain Upgrade Kit: 1.3.0.3/1.2 DiTi Cone. The PrepStain System is a liquid-based thin layer cell preparation process. The PrepStain System produces SurePath Slides that are in
  • Z-2085-2012 · Dec 8, 2011 · Terminated
    PrepStain Kit: 1.2 DiTi Cone. The PrepStain System is a liquid-based thin layer cell preparation process. The PrepStain System produces SurePath Slides that are intended for use i
  • Z-2088-2012 · Dec 8, 2011 · Terminated
    PrepStain PM Kit, T-AG (Catalog 490588); PrepStain PM Kit Europe (Catalog 490671); PrepStain Prep Only PM Kit, T-AG (Catalog 490954); PrepStain PM Kit XLP, T-US-II (Catalog 490424)
  • Z-1090-2009 · Sep 26, 2008 · Terminated
    BD PrepStain System, Model Number: 799-14000-00; Catalog Number: 05CR000021, 05CR00021R, 799-13000-00, 799-13000-00R, 799-14000-00 and 799-14000-00R; Catalog Number: 05CR000021, 05

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Sources and updates

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