Z-2889-2020 Class II Terminated

Recalled by Becton Dickinson & Company — Franklin Lakes, NJ

FDA device recall Z-2889-2020 was initiated by Becton Dickinson & Company on July 28, 2020 and is designated Class II. Reason for recall: Printed scale markings on the 3mL SafetyGlide syringes, with catalog # 305924, Lot# 8289599, are printed incorrectly. The scale is skewed to different degrees, resulting in missing and/or partially pr… The recall status is terminated (terminated April 23, 2021). Affected quantity: 125,200 units.

Recall Details

Product Type
Devices
Report Date
September 2, 2020
Initiation Date
July 28, 2020
Termination Date
April 23, 2021
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
125,200 units

Product Description

BD SafetyGlideTM 3ml 25G x 1 3mL SafetyGlide syringes, 50 units in pack

Reason for Recall

Printed scale markings on the 3mL SafetyGlide syringes, with catalog # 305924, Lot# 8289599, are printed incorrectly. The scale is skewed to different degrees, resulting in missing and/or partially printed scale numbers and scale lines.

Distribution Pattern

US and Canada

Code Information

Catalog #: 305924 Lot #: 8289599 UDI #: 30382903059240