Recalls · Brand

BASE 10 GENETICS INC recalls

Every recall we track for BASE 10 GENETICS INC — 1 in all, all from 2022 — plus the complaints and injury reports the public filed about them.

1recalls

Recalls per year, by danger level

1 recall since 2017.

All FDA recall records for BASE 10 GENETICS INC since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.

Recalls per year for BASE 10 GENETICS INC, by danger level
Year	Not yet rated	Total
2017	0	0
2018	0	0
2019	0	0
2020	0	0
2021	0	0
2022	1	1
2023	0	0
2024	0	0
2025	0	0
2026 (to date)	0	0

What to do if you have a recalled BASE 10 GENETICS INC product

Match the model, catalog or lot number on your device to the recall.
Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
Report problems to FDA MedWatch.

See this week’s new recalls.

All BASE 10 GENETICS INC recalls

1 shown

UnratedMedical device
BASE 10 GENETICS INC recalls RNAstill Molecular Transport Medium Vial, Catalog number MTM-001, a component of the following catalog numbers of
BASE 10 GENETICS recalls RNAstill Molecular Transport Medium Vials (MTM-001) due to lack of 510(k) clearance. These vials are part of specimen collection kits for swab tests. Affected lots include MG18401, MG18409, HH04806, KM02643, MG27906, MG28502, MG30295, MG33903, MG18408, MG27901, and KC28836.
BASE 10 GENETICSJan 10, 2022

BASE 10 GENETICS INC recall questions

How many recalls has BASE 10 GENETICS INC had?

1 recall from BASE 10 GENETICS INC are on record with U.S. safety agencies, from 2022.

What is the most recent BASE 10 GENETICS INC recall?

BASE 10 GENETICS INC recalls RNAstill Molecular Transport Medium Vial, Catalog number MTM-001, a component of the following catalog numbers of, dated Jan 10, 2022. Every BASE 10 GENETICS INC recall is listed on this page, newest first.

What should I do if I have a recalled BASE 10 GENETICS INC product?

Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.

How do I get alerts for new BASE 10 GENETICS INC recalls?

Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.