FDA recall record

Matrix Surgical Holdings OP7543 Design Y Mandible Onlay - Medium - Left and OP7544 Design Y recall — FDA Z-1382-2017

Mislabeling. The packaging labeled as left mandible contained a right mandible.

Class IIclassification
Z-1382-2017official record ID
Mar 8, 2017report date

Recall record at a glance

Official recordZ-1382-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMatrix Surgical Holdings, LLC
Report dateMar 8, 2017
Recall initiation dateJan 25, 2017
Quantity28
LocationAtlanta, GA, United States

Official product description

OP7543 Design Y Mandible Onlay - Medium - Left and OP7544 Design Y Mandible Onlay - Medium - Right

Why the product was recalled

Mislabeling. The packaging labeled as left mandible contained a right mandible.

Distribution information

Worldwide Distribution to the countries of : Brazil, Chile, Colombia, Norway, Saudi Arabia, South Africa, Sweden and Taiwan

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: E-Mail.

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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