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Recall Observatory FDA recall evidence

Device product

Ion Flexison Biopsy Needle, 19G, Extension Range : 0-3 cm, Ref: 490104-09 and 49004-10, 5-pack, Sterile EO, Rx only, UDI:00886874115978

Z-0106-2022

August 06, 2021

Class II

Product summary

Firm
Intuitive Surgical, Inc.
Event
Event 88524
Status
Terminated
Classification
Class II
Quantity
1625 units
Official record key
device-enforcement:Z-0106-2022

Official wording

Reason: Potential for the sheath tip on the biopsy needle to separate from the sheath shaft.

Code information: Affected Lot Number(s): S90200303, S90200622, S90200727, S90200811, S90200820, S90200831 ,S90200909, S90201008, S90201015 ,S90201103, S90201107, S90201125 ,S90201202, S90201204, S90210114 ,S90210211, S90210225, S90210310 ,S90210318, S90210408, S90210414

Distribution pattern: US: AZ, AR, CA, CO, DC, FL, GA, IL, IN, IO, MD, MA, MI, MN, MO, NV, NJ, NY, NC, OH, OK, PA, TN, TX, UT, VA, WA OUS: China

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Potential for the sheath tip on the biopsy needle to separate from the sheath shaft.