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

Recall Z-2598-2018 — BD FACS Universal Loader (Optional) to the BD FACSLyric Clinical System, Model 662879 (Universal Loader), Rx Only. The firm name on the label is Becton, Dickinson and Company, BD Biosciences, San Jose, CA. The Loader offers various settings to resuspend and mix samples. It can draw from 12 x 75

U.S. FDA — Device Enforcement · United States · 2018-05-16 · Class III

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2598-2018
Date of alert: 2018-05-16
Country / jurisdiction: United States
Risk level: Class III
Risk type: recall
Brand: Becton, Dickinson and Company, BD Biosciences
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 2662879000001

Reported risk: The solenoid plunger tip length is too short resulting in insufficient engagement to the Universal Loader enclosure to lock during use.

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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