FDA recall record

Arthrex BioSync Anatomic Cotton Wedge, 20 x 6.5 mm recall — FDA Z-1963-2016

Potential for polystyrene particulate presence.

Class IIclassification
Z-1963-2016official record ID
Jun 22, 2016report date

Recall record at a glance

Official recordZ-1963-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmArthrex, Inc.
Report dateJun 22, 2016
Recall initiation dateApr 22, 2016
Quantity138 total products
LocationNaples, FL, United States

Official product description

BioSync Anatomic Cotton Wedge, 20 x 6.5 mm.; Used for internal bone fixation for bone fractures, fusions or osteotomies in the ankle and foot.

Why the product was recalled

Potential for polystyrene particulate presence.

Distribution information

Distributed in the states of CA, CO, FL, GA, IL, IN, KS, MD, NC, NY, PA, SC, VA, WA, and WI.

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

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.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.