FDA recall record

Neocis DRW-0739-01:Gen 2 Anterior Chairside Splint LRUL (lower right-upper left) recall — FDA Z-0929-2021

The LRUL and LLUR posterior chairside splints and the LLUR anterior chairside splints may be mislabeled.

Class IIclassification
Z-0929-2021official record ID
Feb 3, 2021report date

Recall record at a glance

Official recordZ-0929-2021
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNeocis, Inc.
Report dateFeb 3, 2021
Recall initiation dateOct 30, 2020
Quantity100 units
LocationMiami, FL, United States

Official product description

DRW-0739-01:Gen 2 Anterior Chairside Splint LRUL (lower right-upper left); accessories to the parent system, the Neocis Guidance System (NGS)

Why the product was recalled

The LRUL and LLUR posterior chairside splints and the LLUR anterior chairside splints may be mislabeled.

Distribution information

OH, FL, CT, MA, AZ PA, NY

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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