FDA Device recall Z-2024-2021
Vivorte Trabexus EB 10 cc Bone Void Filler -Fill bone and/or defect in skeletal system Model Number: 130703-10
- FDA Device
- Class II
- terminated
- Published 2021-07-14
On 2021-07-14 the FDA classified a Class II recall of Vivorte Trabexus EB 10 cc Bone Void Filler -Fill bone and/or defect in skeletal system Model Number: 130703-10 by Vivorte, citing incorrect expiration date- product is listed with 02-15-2019 the correct kit expiration date is 12-18-2018.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2024-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-09-09 |
| Published | 2021-07-14 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Vivorte |
| Distribution | KY |
Product
Vivorte Trabexus EB 10 cc Bone Void Filler -Fill bone and/or defect in skeletal system Model Number: 130703-10
Reason
incorrect expiration date- product is listed with 02-15-2019 the correct kit expiration date is 12-18-2018
Identifiers
| code_info | Lot Number: MA-170727-01 Donation Identification Number (DIN): W2292 14 141647 00 Serial Numbers: 093 through 105.…Lot Number: MA-170727-01 Donation Identification Number (DIN): W2292 14 141647 00 Serial Numbers: 093 through 105. Human readable UDI (under QR code on label): =/W4146EB0010T0475=W22921414164700=,000XXX=>019046=}017239&,100000000MA17072701 where XXX ranges from 093 through 105. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2024-2021%22
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