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

Recall Z-2284-2021 — Monoject 0.9% Sodium Chloride Flush Syringe, 10 mL Fill, STERILE, Product Code 8881570121 The proposed device is indicated for use in flushing compatible intravenous tubing systems and indwelling intravascular access devices.

U.S. FDA — Device Enforcement · United States · 2021-08-04 · Class I

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2284-2021
Date of alert: 2021-08-04
Country / jurisdiction: United States
Risk level: Class I
Risk type: recall
Brand: Cardinal Health
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 8881570121

Reported risk: Potential for the plunger to draw back after the air has been expelled and reintroduce air back into the syringe.

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.

Recall Z-2284-2021 — Monoject 0.9% Sodium Chloride Flush Syringe, 10 mL Fill, STERILE, Product Code 8881570121 The proposed device is indicated for use in flushing compatible intravenous tubing systems and indwelling intravascular access devices.

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