Access Scientific LLC: Medical Device Recall in 2020 - (Recall #: Z-1972-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND" ED Quick Kit 3FR 6cm. REF/UDI 72627/ 00859821006674 - Product Usage: is used to gain access to the vascular system to sample blood and administer fluids intravenously. It may be used for power injection of contrast media up to a rate of 8 ml/sec and at a maximum of 325 psi fluid pressure.

Product Classification:

Class II

Date Initiated: April 23, 2020

Date Posted: May 20, 2020

Recall Number: Z-1972-2020

Event ID: 85586

Reason for Recall:

Saline Flush Syringe compromised sterility due to holes in the packaging.

Status: Terminated

Product Quantity: 2697 units

Code Information:

LOT: 257828, 258294, 259262, 260814, 260173, 261861, 264561, 266804, 266805, 267191, 269121

Distribution Pattern:

US Nationwide distribution including in the states of AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, ME, MI, MN, MO, MS, NC, NH, NJ, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, WA.

Voluntary or Mandated:

Voluntary: Firm initiated