Krishe Dasky Disposable Sampling Tubes Recall: FDA Verification Missing
Krishe recalls Dasky Disposable Sampling Tubes (REF VSM02) due to missing FDA verification for virus transport media. All lots affected; no remedy stated.
Recall notice
Verification and validation of the virus transport medium tubes was not provided to FDA prior to sale and marketing
Contact the company
What happened, in plain English
Krishe is recalling Dasky Disposable Sampling Tubes (REF VSM02) because they were sold without proper FDA verification for virus transport media. This could pose a risk if the tubes are used in medical testing without confirmed safety. Read more at govinfonow.com/recall/63101-krishe-dasky-disposable-sampling-tubes-recall-fda-verification-missing.
Source Summary by GovInfoNow · govinfonow.com/recall/63101-krishe-dasky-disposable-sampling-tubes-recall-fda-verification-missing · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1421-2021
Cite this page
“Krishe Dasky Disposable Sampling Tubes Recall: FDA Verification Missing.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/63101-krishe-dasky-disposable-sampling-tubes-recall-fda-verification-missing. Based on FDA recall #Z-1421-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1421-2021%22&limit=1).
Why it’s dangerous
The tubes were sold without FDA verification for virus transport media, meaning their safety and accuracy for medical testing could not be confirmed. This might lead to incorrect test results or unsafe use if the tubes are not properly validated.
Who’s affected
Healthcare workers and labs using Dasky Disposable Sampling Tubes (REF VSM02) are affected. Those using the tubes for medical testing without verified safety may be at risk.
How to tell if you have this one
Check for the Dasky Disposable Sampling Tube with REF VSM02. The product includes 50 transport media, 50 nasal swabs, and a package insert. All lots are affected.
- Brand
Krishe- Category
Medical device
All 4 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
US: LA, TX, FL, GA
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-1420-2021 | Disposable Sampling Tube, REF VSM01, Contents: Transport Media - 50, Nasal Swab - 50, Package Insert - 1, IVD, CE; All Lots | 1,700,000 units |
| Z-1421-2021 | Dasky Disposable Sampling Tube, REF VSM02, Contents: Transport Media - 50, Nasal swab - 50, Package Insert - 1, IVD, CE; All Lots | 441,500 units |
| Z-1422-2021 | Dasky Disposable Sampling Tube, REF VSM03, Contents: Sterile 0.85% Saline - 50, Nasal Swab - 50 , Package Insert - 1, IVD, CE; All Lots | 18,000 units |
| Z-1423-2021 | Dasky Disposable Sampling Tube, REF VSM04 (Saliva Collection Kit + VTM), 10 pcs, IVD, Sterile R; All Lots | 10,000 units |
What to do — step by step
Check Product Details
Identify the product by checking for REF VSM02 on the tube packaging.
Where it went and when
Where it was distributed
Distributed in 4 states.
FDA distribution: “US: LA, TX, FL, GA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida, Georgia, Louisiana, Texas.
Recall timeline
FDA terminated this recall 20 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-1421-2021 (March 11, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1421-2021 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.