Lower riskMedical device recall · FDA · Published October 20, 2021
Microvention Aspiration Syringe Kit Recall: Incorrect US Shipping
Microvention recalls Aspiration Syringe Kit REF MVSK60 shipped to US customers without proper labeling. Affected units have specific lot and UDI codes. Stop using if you have the kit.
“Microvention Aspiration Syringe Kit Recall: Incorrect US Shipping.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/61656-microvention-aspiration-syringe-kit-recall-incorrect-us-shipping. Based on FDA recall #Z-0202-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0202-2022%22&limit=1).
The FDA announced on 2021-10-20 that Microvention Inc. is recalling Aspiration Syringe Kits, REF: MVSK60, because kits labeled for overseas distribution were inadvertently shipped to U.S. customers in Alabama, New York, and Nevada. The recall affects 33 units distributed nationwide.
How to tell if you have it
Brand: Microvention
Product: Aspiration Syringe Kit, REF: MVSK60
Lot code: H2146461
UPC: 00816777025906
The hazard
The hazard is that syringe kits labeled for distribution outside the U.S. were inadvertently shipped to U.S. customers, according to the FDA.
Context
GovInfoNow's records show Microvention Inc. has 15 other recalls on record since 2017-08-07. Recent brand recalls include a 2026-04-30 recall of Bobby Balloon Guide Catheters for balloon pinhole defects and a 2026-04-06 recall of LVIS Stent Devices due to manufacturing errors. Other recent recalls of similar products include the 2025-11-13 Microbiologics KWIK-STIK Quality Control Kit Recall for lot labeling mix-ups, the 2026-02-27 Medline Convenience Kits with Unapproved Syringes recall due to design changes, and the 2026-01-07 Medline Convenience Kits Recall for risk of contaminated sterile products.
How to tell if you have this one
Check for the product reference number MVSK60 on the kit. Look for lot number H2146461 or UDI code (01)00816777025906(11)210727(17)240430(10)H2146461.
Brand
Microvention
Product
Aspiration Syringe Kit, REF: MVSK60
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Details
Verify the product reference number and lot number on the kit to confirm if it is affected.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 3 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide distribution in the states of AL, NY, NV.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Nevada, New York.
Recall timeline
FDA terminated this recall 2.6 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0202-2022 (October 20, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0202-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.