G1 Dissection Tool - 6MM CRS DBALL, 2mm Shaft EXP, M; For cutting and shaping bone including spine and cranium.
Reported: September 28, 2016 Initiated: August 26, 2016 #Z-2840-2016
Product Description
G1 Dissection Tool - 6MM CRS DBALL, 2mm Shaft EXP, M; For cutting and shaping bone including spine and cranium.
Reason for Recall
The firm discovered on March 4, 2016 that several product codes were inadvertently left off of Hold 1503.
Details
- Recalling Firm
- The Anspach Effort, Inc.
- Units Affected
- 69
- Distribution
- AZ, DC, CA, MD, MI, and OR Switzerland
- Location
- Palm Beach Gardens, FL
Frequently Asked Questions
What product was recalled? ▼
G1 Dissection Tool - 6MM CRS DBALL, 2mm Shaft EXP, M; For cutting and shaping bone including spine and cranium.. Recalled by The Anspach Effort, Inc.. Units affected: 69.
Why was this product recalled? ▼
The firm discovered on March 4, 2016 that several product codes were inadvertently left off of Hold 1503.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 28, 2016. Severity: Moderate. Recall number: Z-2840-2016.
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