FDAJune 21, 2017device

Spinal & Epidural Anesthesia Tray. Product Catalog Number: 555172. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

B. Braun Medical Inc. (BBMI) initiated this recall of various BBMI convenience kits containing the 22GA 1-1/2in SafetyGlide Needle due to the presence of loose polypropylene foreign matter was above release specification. This foreign matter has been identified as a product hub material which has been tested for biocompatibility per ISO 10993 during the product development process.

What to do

FDA enforcement status: Terminated

Brands named

b braun medical

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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