FDA recall record

Integra LifeSciences MAYFIELD INFINITY XR2 LOW PROFILE BASE UNIT, Part Number A2079A The recall — FDA Z-2594-2018

There is a potential for the knob assembly in the swivel adapter to fracture/break during use.

Class IIclassification
Z-2594-2018official record ID
Aug 8, 2018report date

Recall record at a glance

Official recordZ-2594-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmIntegra LifeSciences Corp.
Report dateAug 8, 2018
Recall initiation dateJun 29, 2018
Quantity1 units
LocationPlainsboro, NJ, United States

Official product description

MAYFIELD INFINITY XR2 LOW PROFILE BASE UNIT, Part Number A2079A The MAYFIELD Infinity XR2 Base Unit is intended to be used to support a patient during diagnostic examination and/or surgical procedures where a rigid support between surgical table and headrest, or skull clamp is necessary, positional freedom is required and where X-ray imaging modalities will be used.

Why the product was recalled

There is a potential for the knob assembly in the swivel adapter to fracture/break during use.

Distribution information

Worldwide Distribution: US (nationwide) to states of: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, and WV; and to countries of:: Australia, Canada, China, Dominican Republic, Hong Kong, India, Japan, Korea, Malaysia, Mexico, Pakistan, Panama, Peru, Singapore, Sri Lanka, Taiwan, and Thailand.

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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