Becton Dickinson & Company: Medical Device Recall in 2014 - (Recall #: Z-2673-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

BD PosiFlush SF Saline Flush Syringe 0.9 Sodium Chloride Injection, USP 10 mL REF 306553. Intended to be used only for the flushing of indwelling vascular access devices.10 mL BD PosiFlush Normal Saline Flush Syringes are generally compatible for use with syringe pumps.

Product Classification:

Class II

Date Initiated: July 22, 2014

Date Posted: October 1, 2014

Recall Number: Z-2673-2014

Event ID: 69047

Reason for Recall:

BD received some reports of open seals found on the BD Posiflush SF Flush Syringe 10 mL (Ref #306553).

Status: Terminated

Product Quantity: 3,088,320 units

Code Information:

REF #306553 Lot numbers 3024261 - exp 12-2015 3046276 - exp 01-2016 4128353 - exp 04-2017

Distribution Pattern:

Nationwide Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated