Thomas Scientific Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient specimen collection. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient specimen collection.
Brand
Thomas Scientific
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Lots 060620MB1 061420MB2 062120MB1 062220MB2 060620MB2 052220MB1 051820D01 060120D01 061520MA1 062220D02 061720MB1 052720D02 061920E01 052120E01
Thomas Scientific is recalling Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient specimen collection due to The firm is replacing all tubes that were manufactured and distributed prior to Enforcement Discretion Approval.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The firm is replacing all tubes that were manufactured and distributed prior to Enforcement Discretion Approval.
Recommended Action
Per FDA guidance
On 8/31/20, the firm provided FEMA with the recall letter, which was distributed to all affected users. Users were informed that product manufactured and distributed prior to Enforcement Discretion Approval was to be removed. The firm offered to replace any returned product. To report and receive replacement, customers should complete the included VTM Product Replacement Form and return it to QC@ThomasSci.com. Thomas Scientific will replace any product that has been returned. Please contact QC@ThomasSci.com for any requests for field support.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026