FDA recall record

Exactech Optetrak Logic CC 15mm Tibial Augment Screws recall — FDA Z-2704-2017

Missing Screw in carton. Nine (9) serial numbers were identified as being inadvertently packaged as one per carton when two per carton are required.

Class IIclassification
Z-2704-2017official record ID
Jul 19, 2017report date

Recall record at a glance

Official recordZ-2704-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmExactech, Inc.
Report dateJul 19, 2017
Recall initiation dateApr 7, 2017
Quantity9 devices
LocationGainesville, FL, United States

Official product description

Exactech Optetrak Logic CC 15mm Tibial Augment Screws

Why the product was recalled

Missing Screw in carton. Nine (9) serial numbers were identified as being inadvertently packaged as one per carton when two per carton are required.

Distribution information

CA and 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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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