The Recall Desk
HighFDA (Devices)·Z-1978-2020·Announced 2020-05-20

Access Scientific Recalls BD PosiFlush Saline Syringes Due to Packaging Holes

Access Scientific LLC is recalling 30 units of BD PosiFlush SF Saline Flush Syringes because holes in the packaging compromised sterility.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a medical device with compromised sterility, which poses a risk of harm (infection) even though no specific injuries or illnesses are reported in the source text.

Plain-English summary

Access Scientific LLC is recalling 30 units of BD PosiFlush SF Saline Flush Syringe 10 mL used in the POWERWAND XL 5Fr 8cm Quick Kit. The recall was initiated because holes in the packaging compromised the sterility of the syringes.

The affected products are identified by lot numbers 263649 and 268326. These devices are used to gain access to the vascular system to sample blood and administer fluids intravenously, including power injection of contrast media.

The products were distributed nationwide in the United States, 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, and UT. Users should stop using the affected syringes and contact the manufacturer for further instructions.

The recalled product

Product
BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 5Fr 8cm Quick Kit. REF/UDI / 94114/10859821006220 - 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 med
Affected units
30

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • LOTS:263649
  • 268326

Distribution

Distributed nationwide across the United States.

The notice also names 34 states specifically:

Part of a larger recall action

This product is one of 12 recalled by Access Scientific LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 12 products in this recall →