Medagent recalls Rebstock Holding Rod (Art. No. 06-06-285) due to risk of uncontrolled movement affecting patient safety during surgery. Affected units include specific batch numbers.
Holding arm could move (twist) uncontrollably in the front area. This could lead to a serious deterioration of patient's safety if the movement is transferred to the spatula, which is attached to the holding arm.
Medagent is recalling Rebstock Holding Rods for surgical use because they can twist uncontrollably, potentially causing patient injury if the movement transfers to attached surgical tools. This is a serious safety issue for surgical teams using these devices.
The holding rod can twist uncontrollably in the front area. If this movement transfers to the attached spatula, it could cause serious patient injury during surgery. The hazard occurs during normal use when the rod is attached to surgical tools.
Surgical teams using Rebstock Holding Rods for fixing flexible Leyla Arms and spatulas are most at risk. Patients undergoing procedures with these devices could face injury if the rod moves unexpectedly.
Check for the product model number 06-06-285 or 06-06-285MOD. Affected units include specific batch numbers: 6221672, 6222079, 6230282, 6230985, 6230986, 6231808, 6222559, 6231989, 6221673.
Look for model numbers 06-06-285 or 06-06-285MOD on the device.
Reach out to Medagent Inc for assistance with the recall process.
The recall indicates the product can move uncontrollably, posing a risk of patient injury. Do not use until the manufacturer provides guidance.
Affected batch numbers are 6221672, 6222079, 6230282, 6230985, 6230986, 6231808, 6222559, 6231989, 6221673.
The recall record does not specify a replacement process. Contact Medagent Inc directly for assistance.
We’ve drafted a message you can send Medagent to request your refund or repair — edit it as you like.
Subject: Recall Z-1184-2024 — Medagent Medagent Hello, I own a Medagent that is covered by recall Z-1184-2024 from Medagent. 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.
