Devices

Device Recall Anspach BLACKMAXN (Pneumatic motor) and Autolube III

Model / Serial
Serial # 1934, 3135, 50229989-3, and 31496704 (BLACKMAX-N) Serial # 80017906 (Foot Control)
Product Classification
General and Plastic Surgery Devices
Device Class
1
Implanted device?
No
Distribution
US Distribution: Maryland only.
Product Description
Anspach BLACKMAX-N (Pneumatic motor) and Autolube III (Foot Control). || Cutting and shaping bone.
Manufacturer
The Anspach Effort, Inc.
1 Event
- Recall of Device Recall Anspach BLACKMAXN (Pneumatic motor) and Autolube III

Manufacturer

The Anspach Effort, Inc.

Manufacturer Address
The Anspach Effort, Inc., 4500 Riverside Drive, Palm Beach Gardens FL 33410-4235
Manufacturer Parent Company (2017)
Johnson & Johnson
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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