# Major Recall Alert: Dual Mobility Vivacit-E® Vitamin E Bearing Recalled Due to Packaging Discrepancy by Zimmer Biomet
Zimmer Biomet has announced an important recall for one (1) lot of its **Dual Mobility Vivacit-E® Vitamin E Bearing** due to a significant packaging error. The outer package of this medical device is labeled as a **size G 46 mm**, but upon inspection, the implant inside was found to be a **size F 44 mm**, posing a potential risk during surgical procedures. The defect was uncovered on **September 19, 2025**, via the company’s routine complaints handling process, following one (1) reported size discrepancy incident during a procedure.
This recall involves a critical product used in surgical settings, making it vital for healthcare providers, patients, and distributors to stay informed. Keep reading to learn more about this urgent recall and what steps you should take.
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## Why This Recall is Important
The **Dual Mobility Vivacit-E® Vitamin E Bearing** is commonly used in joint replacement surgeries and other orthopedic procedures, where precise sizing is crucial for effective outcomes. The identified packaging error creates a mismatch between the labeled size of the device and the actual implant size. As a result, surgeons may face challenges during procedures, leading to potential delays, safety risks, and patient discomfort.
Zimmer Biomet has confirmed that this packaging issue affects only **one (1) specific lot of the Dual Mobility Vivacit-E® bearing**, but the potential impact on surgical outcomes makes this recall highly significant.
The issue was discovered through standard complaint handling procedures and is a precautionary yet necessary step to ensure patient safety.
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## Details of the Recall
Here are the key details of the Zimmer Biomet recall:
- **Product Name**: Dual Mobility Vivacit-E® Vitamin E Bearing
- **Recall Reason**: Possible commingle between labeled size (G 46 mm) and implant size (F 44 mm).
- **Discovery Date**: The issue was identified on **September 19, 2025**, via a reported complaint.
- **Affected Lot**: One (1) specific lot of the product.
- **Reported Issues**: One (1) incident of size discrepancy identified during a procedure.
- **Location**: Canada-wide recall.
Healthcare professionals and distributors should immediately verify their inventory and isolate any affected products. Visit the official government recall page for further details: [Dual Mobility Vivacit-E® Vitamin E Bearing Recall](https://recalls-rappels.canada.ca/en/alert-recall/dual-mobility-vivacit-er-vitamin-e-bearing).
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## What You Should Do
If you’re a healthcare provider, distributor, or patient potentially affected by this recall, follow these steps:
1. **Check Inventory**: Immediately inspect all Dual Mobility Vivacit-E® devices in stock.
2. **Verify Lot Numbers**: Confirm whether the product matches the affected lot involved in this recall.
3. **Cease Use**: If the product belongs to the recalled lot, discontinue its use immediately.
4. **Contact Zimmer Biomet**: Reach out to Zimmer Biomet customer service for further guidance or to arrange the return of the product.
5. **Seek Medical Advice**: Patients who may have concerns about their implant should contact their healthcare provider promptly.
Reporting additional issues or concerns to Health Canada can provide critical data to ensure better outcomes for other patients.
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## Stay Safe – Get Instant Recall Alerts
Recalls like this one highlight why staying informed about product safety alerts can make a difference. To receive instant notifications on important recalls and safety information, download the **Canada Recalls and Safety Alerts app** today.
Stay proactive and ensure you stay ahead of potential risks—invaluable knowledge is just a click away!
[Download the Canada Recalls App Here](https://recalls-rappels.canada.ca/en/alert-recall/dual-mobility-vivacit-er-vitamin-e-bearing)
_Stay informed. Stay safe._