Becton Dickinson recalls Bard 3F SL PowerMidline Basic Kits that lack the stylet/T-lock assembly, potentially causing procedural delays or kit discards during IV therapy.
Kits do not contain the stylet/T-lock assembly indicated as a component on the label, may lead to a procedural delay and possibly discard of the kit.
Becton Dickinson is recalling Bard 3F SL PowerMidline Basic Kits that do not include the stylet/T-lock assembly listed on the label. This could lead to procedural delays or the need to discard the kit during IV therapy.
The kits are missing the stylet/T-lock assembly that is listed on the label. This could cause procedural delays or the kit being discarded during medical procedures like IV therapy, blood sampling, or contrast injections.
Healthcare professionals using the kit for intravenous therapies, blood sampling, or contrast media injections. Patients receiving care with this kit may be at risk if the kit is used without the required assembly.
Check for the lot number REEP2920 and expiration date January 2022 on the kit. The kit is CE-indicated for short-term peripheral venous access.
Verify the kit includes the stylet/T-lock assembly listed on the label.
The kits do not contain the stylet/T-lock assembly indicated on the label, which may lead to procedural delays or discarding the kit during medical procedures.
The recall record does not specify a remedy, so check if the kit includes the stylet/T-lock assembly and contact Becton Dickinson for further guidance.
The kit may be safe if it includes the stylet/T-lock assembly, but the recall indicates a risk of procedural delays or discarding the kit if the assembly is missing.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-0294-2021 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-0294-2021 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.
