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

Recall Z-1252-2021 — Magellan 3 mL Syringe with Hypodermic Safety Needle, 25 G x 5/8" (0.508 mm x 1.6 cm). A single lumen needle intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. Product Code: 8881833558

U.S. FDA — Device Enforcement · United States · 2021-02-09 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1252-2021
Date of alert: 2021-02-09
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Cardinal Health 200, LLC
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 8881833558

Reported risk: Safety shield not locking into the cannula. If the safety shield activation fails to lock a contaminated needle, a needlestick may occur and there is the potential for exposure to bloodborne pathogens

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-1252-2021 — Magellan 3 mL Syringe with Hypodermic Safety Needle, 25 G x 5/8" (0.508 mm x 1.6 cm). A single lumen needle intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. Product Code: 8881833558

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