Bect: Phoenix AST Indicator (Catalog 246004) with specific batch numbers recalled due to increased test aborts in certain lab panels.
Panels inoculated using certain lots of the indicator solution are demonstrating an increased occurrence of test aborts.
Becton Dickinson is recalling Phoenix AST Indicator devices with specific batch numbers because they cause more frequent test failures. This could lead to inaccurate lab results if used without the recall fix.
The indicator solution in certain batches causes more frequent test aborts when used in lab panels. This means lab results might be inaccurate, potentially affecting patient care decisions.
Lab technicians and healthcare facilities using the Phoenix AST Indicator with the listed batch numbers are most at risk. The recall affects specific lab equipment used in medical testing.
Check the batch number on the Phoenix AST Indicator (Catalog 246004). The affected batches are listed in the recall notice: 8150994, 8143513, 8114664, 8103968, 8101893, 8094599, 8088904, 8254800, 8247722, 8239891, 8236927, 8236686, 8159672, 8156625, 8150957, 8150525.
Look for the batch number on the Phoenix AST Indicator (Catalog 246004) to see if it matches the listed affected batches.
The Phoenix AST Indicator with certain batch numbers causes increased test aborts in lab panels, which could lead to inaccurate lab results.
Check the batch number against the list of affected batches provided in the recall notice. If it matches, stop using it and contact Becton Dickinson for further instructions.
The recall notice does not specify a fix or remedy. Affected users should check the batch number and contact Becton Dickinson for guidance.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-0934-2019 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-0934-2019 from Becton Dickinson. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
