Access Scientific LLC Recall: BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND
Access Scientific LLC Recall: BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Access Scientific LLC; Product: BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 5Fr 8cm Max Barrier Kit. REF/UDI / 94116/1085982100
| Recalling firm | Access Scientific LLC |
|---|---|
| Product | BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 5Fr 8cm Max Barrier Kit. REF/UDI / 94116/10859821006237 - 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. |
| Reason for recall | Saline Flush Syringe compromised sterility due to holes in the packaging. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | 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. |
| Recall initiated | 20200423 |
| Recall number | Z-1983-2020 |
| Category | device |
| State | CA |
| Country | United States |
$29/mo
Try RecallGuard →