Z-2008-2019 Class II Terminated
FDA device recall Z-2008-2019 was initiated by Becton Dickinson & Company on February 1, 2019 and is designated Class II. Reason for recall: 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. The recall status is terminated (terminated June 11, 2020). Affected quantity: 428,800.
Recall Details
- Product Type
- Devices
- Report Date
- July 31, 2019
- Initiation Date
- February 1, 2019
- Termination Date
- June 11, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 428,800
Product Description
3mL Safety-Lok Syringe, Catalog Number 309606, UDI 30382903096061
Reason for Recall
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.
Distribution Pattern
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 distributed to the following foreign countries: Suriname.
Code Information
Lot Number 8307694