Louisville, KY, United States
Vivorte, Inc. recalls
1 recall recorded since 2018, most recently on 9 September 2018. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 9 September 2018
- Terminated
- 17 November 2021
- Reason
- incorrect expiration date- product is listed with 02-15-2019 the correct kit expiration date is 12-18-2018
- Distribution
- US state of KY
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2024-2021
- Vivorte Trabexus EB 10 cc Bone Void Filler -Fill bone and/or defect in skeletal system Model Number: 130703-10
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.