Thomas Scientific: Medical Device Recall in 2020 - (Recall #: Z-0449-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: July 14, 2020

Date Posted: November 25, 2020

Recall Number: Z-0449-2021

Event ID: 86607

Reason for Recall:

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

Status: Ongoing

Product Quantity: 115,800 cs (100 vials/cs)

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.

Voluntary or Mandated:

Voluntary: Firm initiated