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. This could result in inadequate suction and cause a delay in patient care.
DeRoyal Industries
225 recalls • • Categories: Other Medical Devices, Implants & Prosthetics, Surgical Instruments, Infusion Pumps
Class I - Dangerous
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 I - Dangerous
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 or remains active after buttons are released.
Class I - Dangerous
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 or remains active after buttons are released.
Class I - Dangerous
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 or remains active after buttons are released.
Class I - Dangerous
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 or remains active after buttons are released.
Class I - Dangerous
DeRoyal manufactured and distributed Surgical Tracecarts that contain a Nurse Assist 16FR Silver Urine Meter Foley which were subsequently recalled.
Class I - Dangerous
Kit were manufactured and distributed with Edwards Life Sciences TruWave Disposable pressure transducers which were subsequently recalled by Edwards Life Sciences.
Class I - Dangerous
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 I - Dangerous
The outer package seal could be open, or compromised which affects the sterility of the procedure pack inside.
The outer package seal could be open, or compromised which affects the sterility of the procedure pack inside.
Class I - Dangerous
The outer package seal could be open, or compromised which affects the sterility of the procedure pack inside.
Class I - Dangerous
The outer package seal could be open, or compromised which affects the sterility of the procedure pack inside.
The outer package seal could be open, or compromised which affects the sterility of the procedure pack inside.
The custom procedure packs contain light handle covers that have been recalled by another firm.
The custom procedure packs contain light handle covers that have been recalled by another firm.
Class I - Dangerous
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 I - Dangerous
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 wrinkle in the breather seal resulting in a sterile barrier breach.
Class I - Dangerous
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 this occurs, the affected devices will not be able to perform the suction function during use.
Class I - Dangerous
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Class I - Dangerous
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Class I - Dangerous
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Class I - Dangerous
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Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
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Class I - Dangerous
XXX
Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class I - Dangerous
XXX
Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
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Class I - Dangerous
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Class I - Dangerous
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Class I - Dangerous
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Class I - Dangerous
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Class I - Dangerous
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Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
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Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
XXX
Class I - Dangerous
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Class I - Dangerous
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Class I - Dangerous
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Class I - Dangerous
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Class I - Dangerous
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Class I - Dangerous
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