Becton Dickinson recalls Phoenix AST-s Indicator (Catalog 246009) with specific batch numbers due to increased test aborts in certain lab panels. Affected users should check their batch numbers and contact the company for guidance.
Panels inoculated using certain lots of the indicator solution are demonstrating an increased occurrence of test aborts.
Becton Dickinson is recalling Phoenix AST-s Indicator devices with specific batch numbers because panels using these indicators show more frequent test failures. This could lead to inaccurate lab results if the device is used without proper correction.
The indicator solution in certain batches causes more frequent test aborts when used in lab panels. This means lab results might be inaccurate, but it does not pose a direct physical risk to users.
Lab technicians and healthcare facilities using the Phoenix AST-s Indicator with the listed batch numbers are most at risk. The recall affects specific models sold in the U.S. market.
Check the batch number on the Phoenix AST-s Indicator (Catalog 246009) to see if it matches the listed numbers: 8298797, 8254819, 8254817, 8247760, 8247750, 8206530, 8194853, 8156642, 8156638, 8131658, 8103973, 8094595, 8023542, 7354942, 7300813.
Look for the batch number on the Phoenix AST-s Indicator (Catalog 246009) to see if it matches the listed numbers.
The indicator solution in certain batches causes more frequent test aborts in lab panels, which could lead to inaccurate lab results.
Check the batch number on the Phoenix AST-s Indicator (Catalog 246009) to see if it matches the listed numbers. If it does, contact Becton Dickinson for guidance.
No, the recall is for potential inaccurate lab results, not physical injury risks.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-0933-2019 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-0933-2019 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.
