Medical device recalls Moderate risk

Becton Dickinson & Company recalls BD Spinal Anesthesia Tray The BD Spinal Anesthesia Tray is intended for use by professional anesthesiologists to perfor…

Recall date
November 7, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0740-2017
FDA classification
Class II
Brand / firm
Becton Dickinson & Company
Sold / distributed
Nationwide Distribution

Why it was recalled

BD is conducting a voluntary product recall of the BD Spinal Anesthesia Tray, Cat (Ref) 405671, lot B01K089D since a very low number of trays are incorrectly labeled as BD Single Shot Epidural Tray, Cat (Ref) 406069.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

BD Spinal Anesthesia Tray The BD Spinal Anesthesia Tray is intended for use by professional anesthesiologists to perform the spinal anesthesia procedure

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