Product Safety Recalls

Product Recall Tracker

Smith & Nephew Orthopaedics GmbH Recall 90118

Description: INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right

Smith & Nephew Orthopaedics GmbH Recall 90118 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-1133-2022
Event ID90118
Event DescriptionINTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right
Product TypeDevices
DistributionDistributed nationwide to GA, OH, IN, TX, CO, MO, TN, CA, NC, PA and internationally to Canada, Australia.
Quantity17 units
Recall ReasonRight nails were anodized, marked, and labelled as left nails and vice versa
Device Classification20220601
Device Code InfoProduct number: 71676627 (DI: 00885556131633), Batch Number: 21LT56988; 71676628 (DI: 00885556040027), Batch number: 21LT56989
Center Classification Date20220525
Recall Initiation Date20220422
Recalling FirmSmith & Nephew Orthopaedics GmbH
Initial Notification Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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.