Becton Dickinson Recalls 3mL Luer-Lok Syringes With Incorrect Scale Markings
Becton Dickinson is recalling 3mL Luer-Lok syringes because the scale markings were printed incorrectly, resulting in missing or partially printed numbers and lines.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II. The hazard involves incorrect scale markings which could lead to dosing errors, but the source text does not report any illnesses or injuries, fitting the criteria for a moderate severity recall.
Plain-English summary
Becton Dickinson & Company is recalling 3mL Luer-Lok Syringes (Catalog Number 309657, UDI 30382903096573) because the scale markings were printed incorrectly. The scale is skewed to varying degrees, which results in missing and/or partially printed scale numbers and scale lines.
The recall affects 460,800 units of the syringes, specifically Lot Number 8303571. The products were distributed to the following US states: FL, IL, KS, MA, ND, NH, NY, OH, PA, RI, SC, VA, and WI. The products were also distributed to the foreign country of Suriname.
Consumers and healthcare facilities should stop using the affected syringes and contact Becton Dickinson & Company for further instructions.
The recalled product
- Product
- 3mL Luer-Lok Syringe, Catalog Number 309657, UDI 30382903096573
- Manufacturer
- Becton Dickinson & Company
- Category
- Medical Device — Syringes
- Hazard
- Affected units
- 460,800
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot Number 8303571
Distribution
Part of a larger recall action
This product is one of 2 recalled by Becton Dickinson & Company under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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