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

Recall Z-0315-2018 — SafetyGlide Needle, 22GA 1-1/2in, Catalog n. 301701, manufactured by BD, sold in Centurion Convenience Kits. Centurion component code BD17O1NS.

U.S. FDA — Device Enforcement · United States · 2017-07-05 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0315-2018
Date of alert
2017-07-05
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Centurion Medical Products Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
2017032350
Reported risk: Centurion is recalling specific lots of convenience kits, SafetyGlide Needle, 22GA 1-1/2in, manufactured by BD, sold in Centurion Convenience Kits. distributed between May 2016 and June 2017 due to notice received from BD's recall due to particulate that could be expelled out of the needle if used for injection.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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.