Catalog Number NLV-340800G |
Device Problem
Insufficient Information (3190)
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Patient Problems
Muscle Spasm(s) (1966); Pain (1994); Swelling (2091); Weakness (2145)
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Event Date 04/14/2000 |
Event Type
Injury
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Event Description
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It was reported that: the pt complains of pain, swelling, and muscle spasms on both hips.The pt reports pain the center of the hip as well as weakness.
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Manufacturer Narrative
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A review of the device history records indicates that the reported devices were manufactured and accepted into final stock met specifications.The complaint history review indicated that there have been similar events for the reported family.The event was confirmed.A voluntary recall ra 2012-067 was initiated for abgii and rejuvenate modular stems and necks due to the potential risks associated with these devices.The reported event is considered to be under the scope of this recall.
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Search Alerts/Recalls
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