FDA recall record

Exactech Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit recall — FDA Z-0900-2017

Disengaged screw head could potentially not be retained in the Torque Defining Screwdriver.

Class IIclassification
Z-0900-2017official record ID
Dec 28, 2016report date

Recall record at a glance

Official recordZ-0900-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmExactech, Inc.
Report dateDec 28, 2016
Recall initiation dateOct 25, 2016
Quantity2,278 units
LocationGainesville, FL, United States

Official product description

Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit

Why the product was recalled

Disengaged screw head could potentially not be retained in the Torque Defining Screwdriver.

Distribution information

Worldwide Distribution - USA (nationwide) Distribution including Puerto Rico and to the states of : AZ, CA, CO, FL, GA, IA, ID, IL, IN, KS, MD, ME, MN, MO, NC, NJ, NV, NY, OH, OK, OR, PA, SC, TN, VA, WA and WI., and to the countries of : Austria, Australia, Canada, Germany, France, Spain, India, Switzerland, Italy, South Korea, United Kingdom, Brazil, Luxembourg, Greece, Guatemala, Netherlands, South Africa, and Sweden

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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