Zavation recalls bone surgery kits with potential inadequate sterilization. Affected lots include 20071860, 2004988, 19113040, 20071775. Contact for remedy.
Products distributed as sterile may not have been adequately sterilized
Zavation is recalling bone surgery kits that may not have been properly sterilized. This could lead to infections if used in medical procedures. Patients using these kits should contact the manufacturer for details.
Sterilization is critical for medical devices to prevent infections. If products were not adequately sterilized, they could introduce harmful bacteria during surgery.
Orthopedic and spinal surgery patients who used the recalled kits. Medical professionals using these kits for procedures are at risk of infection.
Check the lot numbers: 20071860, 2004988, 19113040, or 20071775. These kits are used in orthopedic or spinal procedures.
Look for the lot numbers 20071860, 2004988, 19113040, or 20071775 on the kit packaging.
The recall states products may not have been adequately sterilized, so they are not safe for use in medical procedures.
Contact Zavation directly to get instructions for the remedy, as the recall record does not specify a remedy.
Check the lot numbers: 20071860, 2004988, 19113040, or 20071775.
We’ve drafted a message you can send Zavation to request your refund or repair — edit it as you like.
Subject: Recall Z-1706-2021 — Zavation Zavation Hello, I own a Zavation that is covered by recall Z-1706-2021 from Zavation. 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.
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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.
