Medicrea, IB3D PL Instruments Set, Rx Only REF: SPS03174
FDA Recall Z-1039-2026 · Posted 2026-01-09
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Recalling FirmMedicrea International
Recall StatusOpen, Classified
Product CodeMAX
Date Initiated2025-10-29
Product Quantity44 units
Reason for Recall
Due to complaints, orthopedic rotation tool handle may untread from the shaft resulting in the inability to rotate implant.
Firm Action
On October 29, 2025, Medtronic issued a Urgent: Medical Device Recall Notification via UPS. Medtronic ask consignees to take the following actions:
1. Immediately identify and quarantine the potentially affected product and instruments set identified in the table above.
2. Your local Medtronic Spine Representative will be contacting you to coordinate the return of potentially affected products and instruments sets.
3. Complete and return the Customer Confirmation Form, even if you do not have any affected product. Please complete all fields, sign the form, and email [email protected].
4. This notice should be passed on to all those who need to be aware within your organization or to any organization where the potentially affected devices have been transferred. Please maintain a copy of this notice in your records.
5. If purchased from a distributor, contact your distributor directly to arrange for the return of the product to your Distributor
Root Cause
Under Investigation by firm
Distribution Pattern
US Nationwide distribution in the states of TN, CA, MN, NC, TX, FL, OH, RI, VA.
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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