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GPS

Exactech, Inc. · Model 521-30-06 · UDI-DI 10885862310033

HAW OLO Prescription

510(k) clearances

42,962

Adverse events (104 deaths)

202

Recalls

246

Facilities

Description

GPS MODIFIED TIBIAL CUTTING BLOCK

Recalls

Date	Firm	Reason
2026-09-24	Stryker Leibinger GmbH & Co. KG	Device may fracture during use at the laser welded joint on the pointer tube. If this happens, loose parts may fall out of the product while the device is inside the patient.
2026-08-31	Medtronic Navigation, Inc.	Sterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to detect and track the spheres.
2026-08-31	Medtronic Navigation, Inc.	Sterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to detect and track the spheres.
2026-08-31	Medtronic Navigation, Inc.	Sterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to detect and track the spheres.
2026-08-31	Medtronic Navigation, Inc.	Sterile Passive spheres and biopsy needle kits contain variation in the reflective material which may affect the ability of the navigation system to detect and track the spheres.
2026-03-19	Elekta, Inc.	Locking mechanisms may not properly secure to the Arc system, resulting in shifting of coordinates during procedures.
2025-11-12	Howmedica Osteonics Corp.	When the device is activated during surgery, the device software issues an error message "Instrument Face Mask (6001385000000) is not valid for this application" resulting in an in
2025-09-30	Elekta, Inc.	Due to increased risk that paint flakes from the engravings may separate from the device and there is the possibility that the flake may inadvertently enter the wound
2024-10-04	FHC, Inc.	A complaint was received (MDR 3002250546-2024-00003) prompting an investigation. The investigation revealed a schematic for a spacer tube which is too long relative to the size of
2024-09-25	Elekta Instrument AB	Elekta has become aware that Disposable Biopsy Needles can contain some microscopic debris on the inside of the biopsy needle. The material in the debris is stainless steel, same m

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.