Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1981-2020 — BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 3Fr 6cm Pediatric Kit. REF/UDI / 94124/10859821006480 - 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

U.S. FDA — Device Enforcement · United States · 2020-04-23 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1981-2020
Date of alert: 2020-04-23
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Access Scientific LLC
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10859821006480

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

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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