FDA recall record

B. Braun Medical Sprotte Spinal Tray / Sprotte Spinal Needle 24 gauge with Introducer Spinal recall — FDA Z-1666-2014

B.Braun Medical, Inc. (BBMI) has received reports of 24 gauge Sprotte Needles that are missing the accompanying introducer needles.

Class IIclassification
Z-1666-2014official record ID
Jun 4, 2014report date

Recall record at a glance

Official recordZ-1666-2014
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmB. Braun Medical, Inc.
Report dateJun 4, 2014
Recall initiation dateApr 3, 2014
Quantity7400
LocationAllentown, PA, United States

Official product description

Sprotte Spinal Tray / Sprotte Spinal Needle 24 gauge with Introducer Spinal injection of anesthetics to provide regional anesthesia

Why the product was recalled

B.Braun Medical, Inc. (BBMI) has received reports of 24 gauge Sprotte Needles that are missing the accompanying introducer needles.

Distribution information

Worldwide Distribution - USA (nationwide) and to Canada.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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