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Recall Observatory FDA recall evidence

Device product

Pencan Spinal Needle Tray. Product Catalog Number: 333865. Local anesthesia of the skin prior to insertion of the regional anesthesia needle.

Z-0569-2018

June 21, 2017

Class II

Product summary

Firm
B. Braun Medical, Inc.
Event
Event 78878
Status
Terminated
Classification
Class II
Quantity
11,920 units
Official record key
device-enforcement:Z-0569-2018

Official wording

Reason: 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.

Code information: 0061483775. 0061486469. 0061519983. 0061525310. 0061529050. 0061531352. 0061535252. 0061540004.

Distribution pattern: US Nationwide Distribution.

Derived failure modes

  • Foreign material or chemical contamination

    reason.foreign_material_chemical_contamination · v1.0.0

    foreign matter