Olympus Resection Sheath Recall - Ceramic Tip Breaking

The FDA has initiated a Class II recall for the Olympus Resection Sheath, Model No. A22041T, due to complaints of the ceramic tip breaking. This recall affects nationwide distribution within the US and is ongoing.

FDA Class II Device Recall: MRI LED Battery Overheating Risk (Z-1436-2026)

The FDA has issued a Class II recall (Z-1436-2026) for MRIMed Inc.'s MRI LED Mobile Exam Light Battery (REF SL-111) due to a risk of overheating, melting, and smoke during charging. The recall affects distribution worldwide, including nationwide in the U.S.

Olympus Inner Sheath Recall - Ceramic Tip Breaking

The FDA has issued a Class II recall for Olympus Inner Sheath, Model No. WA22017A, due to complaints of the ceramic tip breaking during use. This recall impacts distribution nationwide in the US and is ongoing.

Medline Dialysis Kit Recall - Silicone Seal Defects

The FDA has initiated a Class II recall for Medline dialysis kits due to defects in the silicone seal of Tego Connectors. These defects can lead to occluded fluid paths, potentially impacting the ability to inject or withdraw blood products. The recall affects nationwide distribution in the US.

Olympus Resection Sheath Class II Recall

The FDA has issued a Class II recall for the Olympus Resection Sheath (Model No. A22043A) due to complaints of ceramic tip breakage. The recall affects nationwide distribution within the US and is ongoing.

Olympus Inner Sheath Recall - Ceramic Tip Breakage

The FDA has issued a Class II recall for the Olympus Inner Sheath (Model No. A2641) due to complaints of ceramic tip breakage. This recall impacts urological applications distributed nationwide in the US.

Olympus Resection Sheath Recall - Ceramic Tip Breaking

The FDA has initiated a Class II recall for Olympus Resection Sheath (Model No. A22043T) due to complaints of the ceramic tip breaking during urologic applications. The recall affects nationwide distribution within the US.

Olympus Inner Sheath Recall - Ceramic Tip Breaking

The FDA has issued a Class II recall for Olympus Inner Sheath (Model No. A2660) due to complaints of the ceramic tip breaking during use. This recall affects nationwide distribution within the US.

Olympus Device Recall - 26 Fr Sheath Ceramic Tip

The FDA has issued a Class II device recall for Olympus Resection Inner Sheaths (Model No. A22040A) due to complaints of the ceramic tip breaking. The recall affects nationwide distribution within the US and is ongoing.

Medtronic Octopus Nuvo Recall - Tubing Assembly Issue

The FDA has issued a Class II recall for Medtronic Octopus Nuvo Tissue Stabilizer systems due to a manufacturing defect where tubing was incorrectly positioned. This recall impacts nationwide distribution in Florida and Indiana.