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5 reported ongoing
7 records in this archive. Latest source date Jul 20, 2023.
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.
Trocar manufactured with the shaft too long and does not meet manufacturing specifications. As a result, when used with the 30¿ neuroendoscope, a portion of the visual field is obscured.
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of FL, ID, IL, MD, NC, NY, OR, RI, TX.
Incorrect product code marked on the product, etched with product code MD611, however; the correct product code is MD610.
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of DC, MO, PA, TX.
Potential for the spring to become loose and fall out of the device, if the spring falls out during a surgical procedure, it may enter the patient's body.
Class IIReported ongoing
Distribution: US Nationwide distribution in the state of OH.
Mislabeled: Product is marked with GTIN # 04046955299592 however; the correct GTIN # is 04046955299607.
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of CA, OH, NE, NH, FL, PA, TX.
Potential for the incorrect screw to be included in the package.
Class IIReported ongoing
Distribution: GA, TX
Application error problems: Rebalance scope message: 1.Rebalancing process 2.Usage of Robot Recovery: 3. Autofocus not available:
Class IIReported terminated
Distribution: US Distribution to states of: AR, IN, NE and NC
Set screwdriver fails during surgery by deforming at the tip during engagement and manipulation of the implant.
Class IIReported terminated
Distribution: US: CA, FL, GA, IL, OH & MI
These examples come from this result page and are not a ranking of every recall reason.
This archive contains 7 records, including 5 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.