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10 reported ongoing
10 records in this archive. Latest source date Jul 10, 2026.
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.
Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material ductility.
Class IIIReported ongoing
Distribution: US Nationwide distribution i the state of MT.
Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material ductility.
Class IIIReported ongoing
Distribution: US Nationwide distribution i the state of MT.
Paragon 28 received two (2) complaints were received involving breaches in the sterile barrier of the pouch packaging.
Class IIReported ongoing
Distribution: US nationwide, Australia, Canada, The Netherlands, and New Zealand
Fibula nail system intended for use in fixation of fibular fractures and osteotomies, has out of specification thread depths on the fibula nail, so implant may not be able to mate properly with the associated mounting bolt. If nail (implant) cannot properly...
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of NJ, WA, NY, MD, CA, FL, NM, TX, IL, OH, NV, TN, LA.
Medical devices distributed, prior to sterilization
Class IIReported ongoing
Distribution: US:CA OUS: None
Medical devices distributed, prior to sterilization
Class IIReported ongoing
Distribution: US:CA OUS: None
Medical devices distributed, prior to sterilization
Class IIReported ongoing
Distribution: US:CA OUS: None
Suture anchor may break upon insertion, which could lead to potential debris in patient, and delays in surgery.
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of AZ, IN, LA, NJ, TX, WA, NY, MD, WI, OK, KY, MI, OH, CA, FL, KS, PA.
Due to Titanium plasma coating not present implant.
Class IIReported ongoing
Distribution: U.S. Nationwide distribution in the states of AL, CA, GA, IL and KY.
Incorrect labeling; There is potential that the drill packaging contains the incorrect part number.
Class IIReported ongoing
Distribution: International distribution in the country of UK.
These examples come from this result page and are not a ranking of every recall reason.
This archive contains 10 records, including 10 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.