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0 reported ongoing
7 records in this archive. Latest source date Feb 10, 2022.
FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
Proximal end of the driver is oversized in varying degrees, making it difficult to fully connect with and remove from the proximal Nextra implant, causing delay in surgery
Class IIReported terminated
Distribution: Distribution US Nationwide, Japan, and the Netherlands
Proximal end of the driver is oversized in varying degrees, making it difficult to fully connect with and remove from the proximal Nextra implant, causing delay in surgery
Class IIReported terminated
Distribution: Distribution US Nationwide, Japan, and the Netherlands
Proximal end of the driver is oversized in varying degrees, making it difficult to fully connect with and remove from the proximal Nextra implant, causing delay in surgery
Class IIReported terminated
Distribution: Distribution US Nationwide, Japan, and the Netherlands
Proximal end of the driver is oversized in varying degrees, making it difficult to fully connect with and remove from the proximal Nextra implant, causing delay in surgery
Class IIReported terminated
Distribution: Distribution US Nationwide, Japan, and the Netherlands
Proximal end of the driver is oversized in varying degrees, making it difficult to fully connect with and remove from the proximal Nextra implant, causing delay in surgery
Class IIReported terminated
Distribution: Distribution US Nationwide, Japan, and the Netherlands
During insertion of the middle phalanx implant into bone, the driver may deform the implant locking mechanism and result in inadequate mating force between the middle and proximal phalanx implants, resulting in surgical delay, in-situ removal of the implant...
Class IIReported terminated
Distribution: US Nationwide distribution in the states of AZ, IL, GA, LA, MD, NY, PA, TX, WA.
During insertion of the middle phalanx implant into bone, the driver may deform the implant locking mechanism and result in inadequate mating force between the middle and proximal phalanx implants, resulting in surgical delay, in-situ removal of the implant...
Class IIReported terminated
Distribution: US Nationwide distribution in the states of AZ, IL, GA, LA, MD, NY, PA, TX, WA.
These examples come from this result page and are not a ranking of every recall reason.
This archive contains 7 records, including 0 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.
Compare the product, firm and lot, date, model or serial identifiers with the notice. Use the label-check guide if you need help locating an identifier.
A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.
This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. Check source coverage and the agency's current notices.
Use monthly archives or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.