Tribio Implant 7.5mm x 40mm REF M80 SB008 UDI code: (01) 00816125023653(10) EBL10B13C(17) 270630 Tribio" Implant is indicated for use in bony voids or gaps of the skeletal system (i.e. extremities, pelvis and posterolateral spine). These osseous defects are surgically created or result from traumatic injury to the bone and are not intrinsic to the stability of the bony structure.
FDA Recall Z-0540-2026 · Posted 2025-11-18
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Recalling FirmBerkeley Advanced Biomaterials, LLC
Recall StatusOpen, Classified
Product CodeMQV
Date Initiated2025-09-02
Product Quantity62 units
Reason for Recall
Due to incorrect product label (Incorrect product name identified on outer packaging).
Firm Action
Between 09/02/2025 to 10/21/2025, the firm emailed an "URGENT-MEDICAL DEVICE RECALL" Letter to customers informing then that affected Tribio Implants have incorrect outer box labeling. The product itself is not defective, but the packaging label does not accurately reflect the product name. The issue of incorrect labeling on the packaging relates solely to the product description, which mistakenly lists the item as a 'Resorbable Bead kit' instead of its correct designation, 'Tribio" Implant.'
Customers are instructed to:
1. QUARANTINE all affected products immediately.
2. DO NOT USE any implants with the serial numbers listed above.
3. CHECK YOUR INVENTORY against the lot and associated serial number list
provided.
4. Follow the instructions below to return a product.
5. Please complete and sign the attached Field Correction Response Form.
6. Please send the completed and signed form within five (5) business days to one of the
following options:
Mail: Berkeley Advanced Biomaterials.
Attention: Quality Assurance Department
2800 Seventh Street
Berkeley, CA 94710
Email: [email protected]
7. You will receive a Returned Goods Authorization (RGA) by email, which will include
detailed instructions for returning the affected products to Berkeley Advanced
Biomaterials, LLC.
8. Additionally, if you have further distributed this product, please identify your customers
and notify them accordingly.
9. At one point in this product Field Correction, your notification to your customers may be
enhanced by including a copy of this product Field Correction letter.
10. Please contact Berkeley Advanced Biomaterials immediately via the phone number or
email address below to arrange the return of the indicated product.
11. If you have any questions regarding the use of the product, please contact our customer
service department at +1(510) 883-0500, Ext. 15, or email [email protected].
Root Cause
Process control
Distribution Pattern
U.S. Nationwide distribution in the state of TN.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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