Devices

Device Recall Reflex Revision Screwdriver Inner Shaft

Model / Serial
Lot codes: 26719, 047377, 047570, 065167, 06A167, and 072689.
Product Classification
Orthopedic Devices
Device Class
1
Implanted device?
No
Distribution
The product was distributed to 13 Stryker branches/agencies.
Product Description
Reflex Revision Screwdriver Inner Shaft is a orthopedic manual surgical instrument that is a nonpowered, hand held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery. Ref Number 48500900;Non Sterile
Manufacturer
Stryker Spine
1 Event
- Recall of Device Recall Reflex Revision Screwdriver Inner Shaft

Manufacturer

Stryker Spine

Manufacturer Address
Stryker Spine, 2 Pearl Ct, Allendale NJ 07401-1611
Manufacturer Parent Company (2017)
Stryker
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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