FDA recall record

Stanmore Implants Worldwide METS SMILES Total Knee Replacement recall — FDA Z-2553-2016

The manufacturer has identified that the stated Femoral Plateau Plates may not fit into the intended Femoral Knee mating component and thus sit flush upon…

Class IIclassification
Z-2553-2016official record ID
Aug 24, 2016report date

Recall record at a glance

Official recordZ-2553-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmStanmore Implants Worldwide Ltd.
Report dateAug 24, 2016
Recall initiation dateMay 31, 2016
Quantity3 units
LocationBorehamwood, N/A, United Kingdom

Official product description

METS SMILES Total Knee Replacement

Why the product was recalled

The manufacturer has identified that the stated Femoral Plateau Plates may not fit into the intended Femoral Knee mating component and thus sit flush upon the Femoral Knee component prior to implantation.

Distribution information

Directly distributed to TX, further distributed to AL and MS

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.