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174 reported ongoing
181 records in this archive. Latest source date May 18, 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.
Sterile wound dressing, lacks sterility assurance
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of FL & NC.
Due to the inner diameter of the suction tubing connector being smaller than the suction canister lid port connection. This size difference, combined with the durometer of the plastic material, makes the assembly to a suction canister lid port difficult. Th...
Class IIReported ongoing
Distribution: U.S.: IL, MN, NC, PA, and VA O.U.S.: N/A
The tubing may not ensure that the yankauer stays intact, and secure to the tubing / yankauer connection for a tight seal. This could result in inadequate suction and cause delay in patient care.
Class IIReported ongoing
Distribution: U.S.: ND, NY, VA, WV, NJ, TN, OK, TN, GA, OH, MN, AZ, WI, IL, MA, MD, MO, AR, MS, NY, MS, SC, HI, AR, UT, HI, O.U.S.: Kuwait
DeRoyal is recalling certain lots of surgical procedure pack products that contain a Stryker SafeAir Smoke Evacuation Pencil. The recall is due to Stryker receiving reports that the pencil is activating without manual input when plugged into a power source ...
Class IIReported ongoing
Distribution: US Nationwide distribution in the state of OH.
DeRoyal is recalling certain lots of surgical procedure pack products that contain a Stryker SafeAir Smoke Evacuation Pencil. The recall is due to Stryker receiving reports that the pencil is activating without manual input when plugged into a power source ...
Class IIReported ongoing
Distribution: US Nationwide distribution in the state of OH.
DeRoyal is recalling certain lots of surgical procedure pack products that contain a Stryker SafeAir Smoke Evacuation Pencil. The recall is due to Stryker receiving reports that the pencil is activating without manual input when plugged into a power source ...
Class IIReported ongoing
Distribution: US Nationwide distribution in the state of OH.
DeRoyal is recalling certain lots of surgical procedure pack products that contain a Stryker SafeAir Smoke Evacuation Pencil. The recall is due to Stryker receiving reports that the pencil is activating without manual input when plugged into a power source ...
Class IIReported ongoing
Distribution: US Nationwide distribution in the state of OH.
DeRoyal manufactured and distributed Surgical Tracecarts that contain a Nurse Assist 16FR Silver Urine Meter Foley which were subsequently recalled.
Class IReported ongoing
Distribution: Florida
Kit were manufactured and distributed with Edwards Life Sciences TruWave Disposable pressure transducers which were subsequently recalled by Edwards Life Sciences.
Class IIReported ongoing
Distribution: US: Virginia
DeRoyal is recalling certain lots of surgical procedure pack products that contain the B.Braun Medical Norm-Ject 2 Piece Syringe. The recall is due to the potential for the sterile packaging barrier to be damaged due to damage to the luer tip of the syringe.
Class IIReported ongoing
Distribution: Pennsylvania
The outer package seal could be open, or compromised which affects the sterility of the procedure pack inside.
Class IIReported ongoing
Distribution: US Nationwide distribution.
The outer package seal could be open, or compromised which affects the sterility of the procedure pack inside.
Class IIReported ongoing
Distribution: US Nationwide distribution.
The outer package seal could be open, or compromised which affects the sterility of the procedure pack inside.
Class IIReported ongoing
Distribution: US Nationwide distribution.
The outer package seal could be open, or compromised which affects the sterility of the procedure pack inside.
Class IIReported ongoing
Distribution: US Nationwide distribution.
The outer package seal could be open, or compromised which affects the sterility of the procedure pack inside.
Class IIReported ongoing
Distribution: US Nationwide distribution.
The custom procedure packs contain light handle covers that have been recalled by another firm.
Class IIReported ongoing
Distribution: US Nationwide distribution in the state of VA.
The custom procedure packs contain light handle covers that have been recalled by another firm.
Class IIReported ongoing
Distribution: US Nationwide distribution in the state of VA.
The reason for the voluntary recall is due to shrinkage of the canister lid. This shrinkage causes the lid not to contact the outer shell to create a seal and thus, it does not create and hold vacuum.
Class IIReported ongoing
Distribution: US Nationwide distribution in the states of Arizona, Texas, Virginia, Pennsylvania, California, Missouri, North Carolina, Illinois, Indiana, Ohio, Arkansas.
DeRoyal is recalling certain lots of surgical procedure pack products that contain a Medtronic Non-Absorbable Suture. The recall is due to Medtronic determining a manufacturing error in the packaging of the non-absorbable sutures that may cause a gap or wri...
Class IIReported terminated
Distribution: US Nationwide distribution in the states of IL, MO.
DeRoyal is recalling certain lots of surgical procedure pack products that contain a ConMed Foot Controlled Electrosurgical Suction Coagulator. The recall is due to ConMed receiving reports that the suction ports may be occluded on the affected devices. If ...
Class IIReported terminated
Distribution: Distribution in US states of VA, and SC.
These examples come from this result page and are not a ranking of every recall reason.
This archive contains 181 records, including 174 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.