Aspiration Syringe Kit, REF: MVSK60 — FDA record Z-0202-2022

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Oct 20, 2021. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Aspiration Syringe Kit, REF: MVSK60
Reason
Syringe Kits labeled for distribution OUS were inadvertently shipped to US customers.
Classification
Class II
Recalling firm
MICROVENTION INC.
Quantity
33
Agency-reported status
Terminated
Source record identifier
Z-0202-2022

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityLot: H2146461; UDI: (01)00816777025906(11)210727(17)240430(10)H2146461

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

US Nationwide distribution in the states of AL, NY, NV.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Nov 10, 2021
Recall initiation date
Oct 20, 2021
Center classification date
Nov 4, 2021
Termination date
May 15, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

Related records