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8 reported ongoing
12 records in this archive. Latest source date Jul 23, 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.
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
Class IReported ongoing
Distribution: US distribution to states of: IA, VA, MO, KS, FL, OH and LS.
Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.
Class IReported ongoing
Distribution: US distribution to states of: IA, VA, MO, KS, FL, OH and LS.
Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may compromise the component's sterile barrier and if used may lead to localized skin or soft tissue inf...
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of OH, IN, NC.
Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.
Class IIReported ongoing
Distribution: US Nationwide distribution in the state of CA.
Cardiovascular procedure kits contain manifolds, the subject of another recall, that may have particulate within the fluid path, which has the potential to be introduced into blood circulation and become lodged within blood vessels.
Class IReported ongoing
Distribution: US: AZ, CO
Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold"
Class IReported ongoing
Distribution: US distribution to state of: AZ OUS: None
The protective pouches were identified to have been improperly labeled with UDI that is associated with an incorrect GMDN (Global Medical Device Nomenclature) code. These blue foam pouches were misused due to misclassification of the GMDN.
Class IIReported ongoing
Distribution: Nationwide distribution. International distribution to Canada.
The kits contain saline flush syringes which were recalled by the supplier.
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of MN and ND. There as no foreign/military/government distribution.
XXX
Class IIReported terminated
Distribution: US Nationwide distribution in the state of VA.
The Port Access Kits were incorrectly labeled as IV Start Kits on the kit label. The case label was correctly labeled as Port Access Kits.
Class IIReported terminated
Distribution: Distribution was made to MN. There was no foreign/government/military distribution.
Scissors contained debris.
Class IIReported terminated
Distribution: Distribution was made to FL, IL, IN, MA, MD, MO, OH, and VA. There was no foreign/government/military distribution.
The kits were incorrectly labeled with an extended expiration date of 02/21/2024 instead of 02/10/2024.
Class IIReported terminated
Distribution: US Nationwide distribution in the state of Pennsylvania.
These examples come from this result page and are not a ranking of every recall reason.
This archive contains 12 records, including 8 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.