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[Recalled] Sprotte Spinal Tray / Sprotte Spinal Needle 24 gauge with Introducer Spinal injection of anesthetics to provide regional anesthesia — B.Braun Medical, Inc | FDA 2014-04-03

recall fda device united-states

The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.

Recall details

ProductSprotte Spinal Tray / Sprotte Spinal Needle 24 gauge with Introducer Spinal injection of anesthetics to provide regional anesthesia
Brand / manufacturerB. Braun Medical, Inc.
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-1666-2014
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date03 April 2014
EAN / barcode61358613

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: B.Braun Medical, Inc. (BBMI) has received reports of 24 gauge Sprotte Needles that are missing the accompanying introducer needles.

This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from B. Braun Medical, Inc.

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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