Product Safety Recalls

Product Recall Tracker

Acera Surgical Inc Recall 89919

Description: Restrata, Part Number RWM1-2X2

Acera Surgical Inc Recall 89919 Information

StatusCompleted
Mandated?Voluntary: Firm initiated
Recall NumberZ-1030-2022
Event ID89919
Event DescriptionRestrata, Part Number RWM1-2X2
Product TypeDevices
DistributionNationwide
Quantity83 units
Recall ReasonMisprinted expiration date on the shelf-box
Device Classification20220511
Device Code InfoLot Number 51745 UDI (01) 8 52425800 60682 (10) 51745 (17) 220218 (21) 0068
Center Classification Date20220502
Recall Initiation Date20220321
Recalling FirmAcera Surgical Inc
Initial Notification Letter
Similar To

© 2022 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.