Catalog Number 999804652 |
Device Problem
Insufficient Information (3190)
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Patient Problems
Pain (1994); Not Applicable (3189)
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Event Date 04/26/2018 |
Event Type
Injury
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Manufacturer Narrative
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(b)(4).No 510(k) number provided because this implant product code was sold internationally.It was sold in the us under a different product code.The correction/removal reporting number listed applies to the corresponding product code sold domestically.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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Asr revision, asr xl, left.Reason(s) for revision: pain.Doi: (b)(6) 2010; dor: (b)(6), 2018; left hip.
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Manufacturer Narrative
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Product complaint #: (b)(4).Investigation summary: the asr platform was voluntarily recalled from the market in august 2010, and the asr product codes are now considered inactive.Further investigation of this individual incident will not be undertaken.The investigation regarding the root cause(s) and/or corrective actions was conducted under mdd capa (b)(4).Ongoing post market surveillance is conducted per our procedures for this product.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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Search Alerts/Recalls
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