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Recall Observatory FDA recall evidence

Device product

Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient specimen collection.

Z-0449-2021

July 14, 2020

Class II

Product summary

Firm
Thomas Scientific
Event
Event 86607
Status
Ongoing
Classification
Class II
Quantity
115,800 cs (100 vials/cs)
Official record key
device-enforcement:Z-0449-2021

Official wording

Reason: The firm is replacing all tubes that were manufactured and distributed prior to Enforcement Discretion Approval.

Code information: Lots 060620MB1 061420MB2 062120MB1 062220MB2 060620MB2 052220MB1 051820D01 060120D01 061520MA1 062220D02 061720MB1 052720D02 061920E01 052120E01

Distribution pattern: US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KA, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The firm is replacing all tubes that were manufactured and distributed prior to Enforcement Discretion Approval.