Vivorte recalls EB 10 cc Bone Void Filler with incorrect expiration date. Product listed as expiring 02-15-2019 but should expire 12-18-2018. Affected units: Model 130703-10, Lot MA-170727-01, Serial 093-105.
incorrect expiration date- product is listed with 02-15-2019 the correct kit expiration date is 12-18-2018
Vivorte is recalling its Trabexus EB 10 cc Bone Void Filler product due to an incorrect expiration date. The product is listed with an expiration date of February 15, 2019, but the correct expiration date is December 18, 2018. This could lead to improper use if the product is used after its actual expiration date.
The product has an incorrect expiration date listed as February 15, 2019, but the correct expiration date is December 18, 2018. Using the product after its actual expiration date could lead to potential issues with the product's effectiveness or safety.
Patients who received the Vivorte Trabexus EB 10 cc Bone Void Filler product with model number 130703-10, lot number MA-170727-01, and serial numbers 093 through 105 are affected. Medical professionals using this product for bone procedures are most at risk.
Check for model number 130703-10, lot number MA-170727-01, and serial numbers 093 through 105 on the product label. The product is sold under the brand Vivorte for bone procedures.
Verify the expiration date on the product label. The product should expire by December 18, 2018, not February 15, 2019.
The correct expiration date is December 18, 2018, but the product is listed with an expiration date of February 15, 2019.
Model number 130703-10 is affected.
Check for lot number MA-170727-01 and serial numbers 093 through 105 on the product label.
We’ve drafted a message you can send Vivorte to request your refund or repair — edit it as you like.
Subject: Recall Z-2024-2021 — Vivorte Vivorte Hello, I own a Vivorte that is covered by recall Z-2024-2021 from Vivorte. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
