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

Recall Z-2183-2013 — Monoject 10 Units/mL Heparin Lock Flush, 12 mL Syringe with 5 mL Fill Product ID: 8881580125 Product Usage: Both 0.9% Sodium Chloride Flush syringes and 10U/mL or 100U/mL Heparin Lock Flush syringes are sterile, single-use products which are intended for use in flushing and locking compatible i

U.S. FDA — Device Enforcement · United States · 2013-08-16 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2183-2013
Date of alert: 2013-08-16
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Covidien LLC
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 8881580125

Reported risk: Monoject prefill flush syringes may contain non-sterile water and labeled as saline or heparin

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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