Product Safety Recalls

Product Recall Tracker

Howmedica Osteonics Corp. Recall 89456

Description: 32MM -4 V40 TAPER VIT HEAD, Catalog Number 6260-5-032

Howmedica Osteonics Corp. Recall 89456 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-0644-2022
Event ID89456
Event Description32MM -4 V40 TAPER VIT HEAD, Catalog Number 6260-5-032
Product TypeDevices
DistributionWorldwide distribution - US Puerto Rico and the countries of Canada, and Malaysia.
Quantity8 units
Recall ReasonThere is a potential for the outer Tyvek lid to de-bond from the sealed package.
Device Classification20220223
Device Code InfoUDI: 07613327012842; Lot Number: 87327407
Center Classification Date20220216
Recall Initiation Date20211221
Recalling FirmHowmedica Osteonics Corp.
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.