Becton Dickinson & Company: Medical Device Recall in 2016 - (Recall #: Z-1936-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Henry Schein Single Use Syringe Luer-Lock, 10 mL, Intended for use by health care professionals for general purpose fluid aspiration/injection

Product Classification:

Class II

Date Initiated: March 25, 2016

Date Posted: June 15, 2016

Recall Number: Z-1936-2016

Event ID: 73828

Reason for Recall:

BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm x 25 mm) and Henry Schein 10 mL Single Use Syringe Luer-Lock are being recalled due to possible adulteration and non-conforming manufacturing practices.

Status: Terminated

Product Quantity: 176,000 units

Code Information:

Catalog (REF #) 9004476, Lot #4163707

Distribution Pattern:

Nationwide Distribution to NY only

Voluntary or Mandated:

Voluntary: Firm initiated