Becton Dickinson recalls Bard 3F SL PowerMidline Full Kits due to missing stylet/T-lock assembly, which could lead to procedural delays or kit discards during IV procedures.
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 Full Kits because they lack the stylet/T-lock assembly listed on the label. This could cause delays or the need to discard the kit during medical procedures.
The kits do not include the stylet/T-lock assembly that is listed on the label. This missing component could cause procedural delays or the need to discard the kit during medical procedures, potentially affecting treatment timelines.
Healthcare professionals using the Bard 3F SL PowerMidline Full Kit for IV access are most at risk. Patients receiving these kits may also be affected if the kit is used incorrectly.
Check for the Bard 3F SL PowerMidline Full Kit with lot numbers REEQ3598 (Feb 2022) or REER0518 (Mar 2022). The kit is CE-indicated for short-term IV access.
Verify that 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 the kit contents to ensure it includes the stylet/T-lock assembly.
The recall indicates a risk of procedural delays or discarding the kit if the stylet/T-lock assembly is missing, but the record does not state the kit is unsafe for normal use.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-0295-2021 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-0295-2021 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.
