Becton Dickinson recalls 3mL Luer-Lok Syringes with incorrect scale markings that may lead to inaccurate dosing. Affected units include Catalog Number 309657, UDI 30382903096573, and Lot Number 8303571.
The syringes have scale markings that were printed incorrectly. The scale is skewed to varying degrees, resulting in missing and/or partially printed scale numbers and scale lines.
Becton Dickinson is recalling 3mL Luer-Lok Syringes with incorrectly printed scale markings. This could cause inaccurate dosing during medical procedures, potentially leading to incorrect medication administration.
The scale markings on the syringes are printed incorrectly, causing missing or partially printed numbers and lines. This can lead to inaccurate measurement of medication doses, which may result in incorrect dosing during medical procedures.
Healthcare professionals and patients using the recalled syringes for medical injections may be affected. Those administering medications with these syringes are at risk of inaccurate dosing.
Check for the Catalog Number 309657 and Unique Device Identifier (UDI) 30382903096573 on the syringe. The affected lot number is 8303571.
Verify the Catalog Number 309657 and UDI 30382903096573 on the syringe. The affected lot number is 8303571.
The syringes have scale markings that were printed incorrectly, resulting in missing or partially printed scale numbers and lines.
Check for the Catalog Number 309657 and Unique Device Identifier (UDI) 30382903096573. The affected lot number is 8303571.
The recall record does not specify a remedy, so no action is required beyond checking the syringe details.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2007-2019 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2007-2019 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.
