Farabeuf Clamp for 3.5mm Screws PRO, Catalog # 705463
Reported: June 27, 2018 Initiated: May 4, 2018 #Z-2244-2018
Product Description
Farabeuf Clamp for 3.5mm Screws PRO, Catalog # 705463
Reason for Recall
Laser etching which indicates whether the device is in compression or distraction mode appears to be on the wrong side of the lever arm
Details
- Recalling Firm
- Stryker GmbH
- Units Affected
- 18 parts (10 parts quarantined)
- Distribution
- AR, CA, ID, IL, MD, MI, NJ, NY, OK, SD & TX
- Location
- Selzach, N/A
Frequently Asked Questions
What product was recalled? ▼
Farabeuf Clamp for 3.5mm Screws PRO, Catalog # 705463. Recalled by Stryker GmbH. Units affected: 18 parts (10 parts quarantined).
Why was this product recalled? ▼
Laser etching which indicates whether the device is in compression or distraction mode appears to be on the wrong side of the lever arm
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 27, 2018. Severity: Moderate. Recall number: Z-2244-2018.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11