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RecallWatchMedical Device Safety
Class IIOngoingZ-1008-2025

Integrity Implants Inc. recalls Brand Name: N/A Product Name: Repeater Bone Tamp Model/Catalog Number: ASY-00132 Sof…

Integrity Implants Inc.Palm Beach Gardens, FL, United StatesReported Jan 29, 2025 · 1 year ago
Legal News Analyst ·

Reason for recall

Due to incompatibility of bone tamp (Rev A) and bone funnels (Rev C).

Affected product

Check your device

Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.

Affected products & lots

  • Brand Name: N/A Product Name: Repeater Bone Tamp Model/Catalog Number: ASY-00132 Software Version: N/A Product Description: The Repeater Bone Tamp is a cylindrical shaft used to push bone graft material through a corresponding bone funnel into the FlareHawk interbody fusion device in spinal fusion procedures. Component: No
    UDI Number
    2 affected lots
    ASY-0013203200045

What the firm is doing

On 12/20/2024, the firm emailed a "NOTICE OF RECALL" letter to customer informing them that the firm has received a report relating to a specific lot of Repeater Bone Tamps not fitting with newer lots of the Repeater Bone Funnel. Customers are instructed to: 1. Segregate Product. immediately remove all Repeater Bone Tamp (Part # ASY-00132, Lot Number 03200045), from their inventory (regardless of its location) and segregate this product in a secure location for return to Accelus. 2. Complete QF-00070 Product Tracking & Verification Form. Complete and return the enclosed QF-00070 Product Tracking & Verification Form (even if you do not have any product to return), following the directions on this page and QF-00070 Product Tracking & Verification Form. Accelus' customer service representative can assist in completing the form. 3. Indicate Returned Products on QF-00070 Product Tracking & Verification Form. QF-00070 Product Tracking & Verification Form lists the Repeater Bone Tamp and product descriptions. Mark the number of each type of Repeater Bone Tamp that will be returned on this form. 4. Call (561)529-3861 or 1-800-201-9300 from 8:30am to 5pm (EDT) should there be any questions about returning the product. Customer's Accelus account will be credited in an amount equal to the actual purchase price for the returned product, if applicable. Inform Customer Service Representative whether customers would like to order a replacement product. 5. Package the Return Material. Package Repeater Bone Tamp(s) that are being returned in an appropriate shipping box. Place a signed original copy of QF-00070 Product Tracking & Verification Form in the box, appropriately seal the box and send it on or before 12-26-2024, to: Accelus 354 Hiatt Drive, Suite 100 Palm Beach Gardens, FL 33418 Office: (561)529-3861 or 1-800-201-9300 Fax: (561) 529-3869

DistributionShow details

U.S. Nationwide distribution in the states of CA, F, GA, KY, LA, MA, MD, TN and VA.

Class IIWhat this means

Use of the product may cause temporary or medically reversible adverse health consequences.

Sources & references

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.

Taylor Coteus
Legal News Analyst

Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.

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