BIOMET 3i LTX DENTAL IMPLANTS Model LTX610 (6x10mm) - Plastic tray within Tyvek tray within cardboard box; one (1) unit per box. Labeled Sterile"
Recall
- Recall Number
- Z-1701-2017
- Event Number
- 76809
- Firm
- Biomet 3i, LLC
- FEI Number
- 1038806
- Product Code
- DZE
- Status
- Terminated
- Root Cause
- Under Investigation by firm
- Initiated
- March 8, 2017
- Terminated
- August 2, 2019
- Address
- 4555 Riverside Dr, Palm Beach Gardens, FL, 33410-4200
Description
BIOMET 3i LTX DENTAL IMPLANTS Model LTX610 (6x10mm) - Plastic tray within Tyvek tray within cardboard box; one (1) unit per box. Labeled Sterile"
A single lot of product that potentially has a single part within the lot that does not match the product on the label due to a commingle at the firm supplier
On March 13 Zimmer Biomet contacted their international consignee and asked them to: 1. Review this notification and ensure affected team members are aware of the contents. 2. Immediately locate and quarantine affected product in your inventory. 3. Complete the Certification of Acknowledgement portion of Attachment 1 Inventory Return Certification Form. a. Return a digital copy to [email protected] within three (3) days. 4. Immediately return all affected product from your distributorship within your territory along with a completed Attachment 1 Inventory Return Certification Form to Biomet 3i. a. For each return, send a copy of Attachment 1 to [email protected]. b. Include a hardcopy of Attachment 1 with your shipment for immediate processing. c. Mark the outside of the returns box(es) clearly with RECALL. 5. Retain a copy of your recall acknowledgement and product return forms for your records in the event of a compliance audit of your facility. If after reviewing this notice you have further questions or concerns please contact us by email at [email protected]. 1-800-342-5454
Argentina
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