Catalog Number UNK HIP FEMORAL SLEEVE ASR |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Fatigue (1849); Foreign Body Reaction (1868); Inflammation (1932); Pain (1994); Loss of Range of Motion (2032); Dizziness (2194); Anxiety (2328); Distress (2329); Discomfort (2330); Deformity/ Disfigurement (2360); Depression (2361); Numbness (2415); Metal Related Pathology (4530); Swelling/ Edema (4577)
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Event Date 03/28/2022 |
Event Type
Injury
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Event Description
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Asr litigation record received.Litigation alleges severe pain, discomfort, elevated metal levels cobalt and chromium, emotional distress, permanent injuries, disability, disfigurement and economic damages.Doi: (b)(6) 2009; dor: (b)(6) 2022; left hip.
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Manufacturer Narrative
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Product complaint # (b)(4).Initial reporter occupation: lawyer.Depuy synthes is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
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Event Description
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Plaintiff form and medical records.After review of medical records patient was revised due to metallosis and failed right total hip arthroplasty.Operative notes indicated that there was not much ingrowth around the cup and the cup came out easily.
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Manufacturer Narrative
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Product complaint # (b)(4).This report is being submitted pursuant to the provisions of 21 cfr, part 803.This report may be based on information which has not been investigated or verified prior to the required reporting date.This report does not reflect a conclusion by depuy synthes joint reconstruction, or its employees that the report constitutes an admission that the product, depuy synthes joint reconstruction, or its employees caused or contributed to the potential event described in this report.If information is obtained that was not available for the initial report, a follow-up report will be filed as appropriate.
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Manufacturer Narrative
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Product complaint # (b)(4).Investigation summary: no device associated with this report was received for examination.This hip replacement platform was voluntarily recalled from the market and the product codes are now considered inactive.Depuy considers the investigation closed.Should additional information be received, the information will be reviewed and the investigation will be re-opened as necessary.Device history lot: device history reviews for asr platform have shown no indication of deviations or anomalies with regard to material, manufacturing or inspection.
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Manufacturer Narrative
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Product complaint # (b)(4).Investigation summary no device associated with this report was received for examination.This hip replacement platform was voluntarily recalled from the market and the product codes are now considered inactive.Depuy considers the investigation closed.Should additional information be received, the information will be reviewed and the investigation will be re-opened as necessary.Update received on 30-november-2022 did not have any additional details to be added in investigation.Depuy considers the investigation closed.Should additional information be received, the information will be reviewed and the investigation will be re-opened as necessary.Device history lot device history reviews for asr platform have shown no indication of deviations or anomalies with regard to material, manufacturing or inspection.H10 additional narrative:.
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Event Description
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Pfs alleges pain, soreness and discomfort along the front right thigh region.Further alleged puffiness, swelling in the right ankle, decrease stamina, endurance, limited mobility, anxiety, fear of elevated metal ions, metallosis, dizziness, numbness/tingling along the toes and fingers, weakness, tiredness and change in gait, limited adl, emotional distress and depression.
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Search Alerts/Recalls
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