Product Safety Recalls

Product Recall Tracker

MICROVENTION INC. Recall 88892

Description: Aspiration Syringe Kit, REF: MVSK60

MICROVENTION INC. Recall 88892 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-0202-2022
Event ID88892
Event DescriptionAspiration Syringe Kit, REF: MVSK60
Product TypeDevices
DistributionUS Nationwide distribution in the states of AL, NY, NV.
Quantity33
Recall ReasonSyringe Kits labeled for distribution OUS were inadvertently shipped to US customers.
Device Classification20211110
Device Code InfoLot: H2146461; UDI: (01)00816777025906(11)210727(17)240430(10)H2146461
Center Classification Date20211104
Recall Initiation Date20211020
Recalling FirmMICROVENTION INC.
Initial Notification Letter
Similar To

© 2021 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied.
Recall.report is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.