Becton Dickinson recalls 3mL Safety-Lok Syringes with incorrect scale markings that may lead to inaccurate dosing. Affected units have catalog number 309606 and UDI 30382903096061.
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 Safety-Lok Syringes with incorrectly printed scale markings. This could cause inaccurate dosing during medical procedures, potentially leading to incorrect medication amounts.
The scale markings are printed incorrectly, causing missing or partially printed numbers and lines. This could lead to inaccurate dosing of medication, especially in critical medical situations.
Healthcare professionals and patients using the recalled syringes for medical injections. Those administering medication with the affected syringes are most at risk.
Check for the catalog number 309606 and unique device identifier (UDI) 30382903096061 on the syringe. The affected units were sold with lot number 8307694.
Verify the catalog number 309606 and UDI 30382903096061 on the syringe. If present, it is affected.
The syringes have scale markings that were printed incorrectly, resulting in missing or partially printed scale numbers and lines.
Check for the catalog number 309606 and unique device identifier (UDI) 30382903096061. Affected units were sold with lot number 8307694.
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-2008-2019 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2008-2019 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.
