# Major Recall Alert: Needle Holder Recalled Due to Product Identification Discrepancy
If you use or work with needle holders, this recent product recall is crucial. A popular **Needle Holder** brand has been officially recalled due to a **product identification discrepancy**. Though marketed and intended as a reusable device, a stamp on the instrument incorrectly indicates **“single use only”**, leading to potential confusion among medical professionals and users. The recall began on **June 27, 2025**, and affects a significant number of devices.
This recall highlights a critical safety concern in medical settings and underscores the importance of adhering to proper device labeling and usage guidelines.
Learn more about the situation below, and make sure to take the necessary steps if this product is in your inventory.
## Why This Recall is Important
The discrepancy over whether the **Needle Holder** is reusable or single-use raises alarms over both patient and practitioner safety. Incorrect use of medical tools due to labeling errors can compromise sterilization standards, increasing risks of contamination, infection, and procedural failures.
When medical instruments are mislabeled, professionals could inadvertently dispose of a reusable product or, worse, reuse a device marked as single-use, which could have devastating consequences.
This issue also emphasizes the manufacturer’s responsibility to ensure product clarity. By addressing the recall, healthcare providers can take timely action, prevent errors in medical protocols, and maintain the highest standard of care.
## Details of the Recall
Here's what we know about the **Needle Holder recall**:
- **Product Affected**: Needle Holder
- **Brand**: Needle Holder
- **Recall Category**: CAN – Product Identification Discrepancy
- **Reason for Recall**: The device is intended to be reusable, but it is incorrectly stamped as a “single-use only” product, which may lead to misuse.
- **Recall Start Date**: June 27, 2025
- **Safety Implications**: Potential misuse due to mislabeled instructions can result in ineffective sterilization or accidents during procedures. This poses a risk to both healthcare providers and patients.
- **Image of Product**: [View Product Image](https://myrecalls.app/images/products/29287_1752195807.jpg)
For the official recall notice and more details, visit [Canada's Recall and Safety Alert Page](https://recalls-rappels.canada.ca/en/alert-recall/needle-holder).
## What You Should Do
If you or your organization uses the **Needle Holder**, here are the steps you need to take immediately:
1. **Identify the Product**: Check your inventory or tools to confirm whether you're using the affected Needle Holder labeled for "single use only."
2. **Cease Use Immediately**: Stop using the product if it’s affected by the recall.
3. **Contact the Manufacturer**: Reach out to the distributor or manufacturer for guidance on replacements, refunds, or corrections.
4. **Follow Disposal Guidelines**: Ensure the device is safely discarded if deemed unsuitable for further use.
If you're in a healthcare setting, inform all staff members about the recall to reduce the risk of inadvertent error.
## Stay Safe – Get Instant Recall Alerts
Avoid missing critical product safety updates by staying informed. Recalls like this one can have significant safety implications, but acting quickly minimizes risks.
**Download the [MyRecalls App](#) now to receive real-time recall alerts directly on your device.** With the app, you’ll stay up-to-date on medical product recalls, automotive alerts, food safety warnings, and more. Be proactive and protect yourself, your patients, and your community today.
For more detailed information about this recall, visit [Canada’s Official Recall Page](https://recalls-rappels.canada.ca/en/alert-recall/needle-holder).
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By staying vigilant and informed, you can ensure that every tool and product in use meets the highest safety standards. Don’t wait—act today to prevent unnecessary risks.