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Upon insertion of a new (unused) Ligasure™ device, the Valleylab™ FT10 energy platform running software versions 4.0.1, 4.0.2 and 4.0.3 may erroneously indicate that the Ligasure™ device was used previously. When this occurs, the energy platform will…

BD continues to receive complaints for the product regarding mismatch between the coaxial and the needle in mission kit devices.  Based on the event reported, the internal diameter of the coaxial cannula may be smaller or larger than the external…

In the identified lot number range of administration sets, the tubing outer diameter may vary in size. Additionally, the length of the tubing which contacts the air sensor may be too short resulting in the need to stretch the tubing to properly fit…

In the identified lot number range of administration sets, the tubing outer diameter may vary in size. Additionally, the length of the tubing which contacts the air sensor may be too short resulting in the need to stretch the tubing to properly fit…

Specific lots of Cardinal Health Monoject™ luer-lock tip syringes (6 and 35 ml) have demonstrated recognition and compatibility issues with certain syringe infusion pumps. As a result, Cardinal Health recommends that they not be used with syringe…

Olympus found that certain lots of the CV-190 do not start up properly and as a result, the image from the endoscope is not displayed when the operations listed below are performed because parts that deviated from the specification were assembled into…

The shaft and tip component of the Universal Joint Screwdriver was manufactured with the incorrect raw stainless steel material. Recall start date: September 1, 2023

Smart tags (bluetooth powered tracking devices) were placed in multiple loaner devices manufactured by Stryker Endoscopy without undergoing verification and validation testing to ensure no adverse effect on product functionality. Recall start date:…

The tracheal intubation scopes, LF-V and LF-P, have been listed as compatible with Olympus endoscope reprocessors (models OER-pro and OER-elite). the OER-pro endoscope reprocessor was the first Olympus model introduced among this series and was launched…

The 9-inch image intensifier for the impacted systems can become detached if the systems encounter a large impact force when moved.  Recall start date: May 25, 2023

Siemens Healthcare Diagnostics Inc. has confirmed the occurrence of discrepant high glucose results in samples with glucose results on the lower end of the reportable range (at or below 54 mg/dl) when using the above listed lots of BGEM test cards in…

There is the potential that an incorrect type of secondary latch could have been installed on the northeast (ne) and/or northwest (nw) bedside panels for certain Giraffe Omnibed Carestation devices (serial number specific). With the incorrect type of…

BD has received complaints regarding mismatch between the coaxial and the needle in mission kit devices, where the coaxial cannula internal diameter and length exceed the external diameter and length of the biopsy needle, prohibiting the biopsy needle…

Medtronic is initiating a voluntary recall for specific production lots of Shiley™ Adult Flexible Tracheostomy Tubes with Taperguard™ Cuff and Cuffless with disposable or reusable inner cannulas. This recall follows reports from customers that the device…

Steris identified through customer complaints that the LB53 light handle covers may separate from the light handle (detach and fall off) during use. Through additional investigation Steris has determined the issue to be associated with the specific lots…