FDA recall record

Synthes (USA) Products Titanium Low Profile Neuro Screw, Self Drilling, 3mm, part numbers recall — FDA Z-1327-2016

Out of specification at the thread. The thread height of these screws is under-sized. The cross section of the affected area is less than that of…

Class IIclassification
Z-1327-2016official record ID
Apr 13, 2016report date

Recall record at a glance

Official recordZ-1327-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSynthes (USA) Products LLC
Report dateApr 13, 2016
Recall initiation dateFeb 23, 2016
Quantity150 units distributed in US, 1439 units distributed OUS (foreign)
LocationWest Chester, PA, United States

Official product description

Titanium Low Profile Neuro Screw, Self Drilling, 3mm, part numbers: 400.833, 400.833E Product Usage: The Low Profile Neuro Plating System is intended for use in selective trauma of the midface and craniofacial skeleton; craniofacial surgery; reconstructive procedures; and selective orthognathic surgery of the maxilla and chin.

Why the product was recalled

Out of specification at the thread. The thread height of these screws is under-sized. The cross section of the affected area is less than that of conforming screws such that the thread height of the screws is undersized.

Distribution information

Worldwide Distribution - US Nationwide in the states of MA, VA, TN, GA, WA, IA, NJ, TN, PA, NY, CO, CT, VT, and the countries of Canada and Switzerland.

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

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