Becton Dickinson recalls Phoenix AP AST Indicator Bags with specific batch numbers due to increased test aborts in certain indicator solutions. Affected units may cause unreliable test results.
Panels inoculated using certain lots of the indicator solution are demonstrating an increased occurrence of test aborts.
Becton Dickinson is recalling Phoenix AP AST Indicator Bags with specific batch numbers because panels inoculated with certain lots of the indicator solution show more frequent test aborts. This could lead to unreliable test results in laboratory settings.
The indicator solution in certain batches causes more frequent test aborts when used in laboratory testing. This means the test results may be unreliable, but it does not pose a direct physical risk to users.
Laboratory users who own or use Phoenix AP AST Indicator Bags with the listed batch numbers are affected. Those conducting microbiological testing with these bags face the highest risk.
Check the batch number on the bag, which is listed in the recall notice (8234684, 8234533, 8225579, and other numbers). These bags were sold with specific batch numbers between the dates mentioned in the recall.
Look for the batch number on the bag, which should match one of the listed numbers (e.g., 8234684, 8234533).
The indicator solution in certain batches causes more frequent test aborts, leading to unreliable test results in laboratory settings.
Check the batch number on the bag. If it matches one of the listed numbers, contact Becton Dickinson for further instructions.
No direct physical risk to users is mentioned; the issue is with test reliability, not safety.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-0935-2019 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-0935-2019 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
