FDA recall record

Epic Extremity Plate System,10x10 Plate Caddy, Part 2111-1010 with 2.7 and 3.5mm Non-Locking recall — FDA Z-1875-2018

There is an error in the caddy artwork that misidentifies a specific plate and screw.

Class IIclassification
Z-1875-2018official record ID
May 23, 2018report date

Recall record at a glance

Official recordZ-1875-2018
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmEpic Extremity, LLC
Report dateMay 23, 2018
Recall initiation dateMar 20, 2018
Quantity9 units
LocationCranberry Twp, PA, United States

Official product description

Epic Extremity Plate System,10x10 Plate Caddy, Part 2111-1010 with 2.7 and 3.5mm Non-Locking Screw (2001-27XX-N & 2001-35XX-N)

Why the product was recalled

There is an error in the caddy artwork that misidentifies a specific plate and screw.

Distribution information

The products were distributed to the following US states: FL, PA, and VA.

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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