Encore Medical recalls djosurgical Linear Neck Trials with Spring Sides due to potential retaining ring failure. Affected models include REF S-200635 and S-200636. No remedy specified in recall notice.
The retaining ring on the neck trials has a potential to fail interoperatively.
Encore Medical is recalling djosurgical Linear Neck Trials with Spring Sides (both standard and lateral versions) because the retaining ring might fail. This could lead to improper use during surgery if the ring breaks. The recall covers specific model numbers and revisions.
The retaining ring on these surgical devices might fail during use, which could cause the device to become unstable or malfunction. This could lead to complications during surgery if the device does not function as intended.
Surgical professionals using djosurgical Linear Neck Trials with Spring Sides for procedures. The risk is highest for those using the recalled models without proper checks.
Check the label for the manufacturer name 'djosurgical' and model numbers REF S-200635 (standard) or REF S-200636 (lateral). The recall includes Revision C trials and specific part numbers like 313R1000, 313R1900, etc.
Look for the manufacturer name 'djosurgical' and model numbers REF S-200635 or REF S-200636 on the device label.
The recall includes djosurgical Linear Neck Trials with Spring Sides, Standard (REF S-200635) and Lateral (REF S-200636), all Revision C models with specific part numbers.
The recall notice does not specify any remedy or action for affected devices.
Check the device label for the manufacturer name 'djosurgical' and model numbers REF S-200635 or REF S-200636.
We’ve drafted a message you can send djosurgical to request your refund or repair — edit it as you like.
Subject: Recall Z-1692-2020 — djosurgical djosurgical Hello, I own a djosurgical that is covered by recall Z-1692-2020 from djosurgical. 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.
