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Respirator requires a disclaimer that it is not NIOSH N95 and to include a unique identifier for each model on the packaging.   Recall start date: 2021-10-27…

When we imported these items 18 months ago, we provided the test results for the KN95 but later learned these results were from the correct manufacturer but for a different model or size. We have no reason to suspect they are bad but now…

Cardinal health is conducting this recall due to the potential for open packaging seals for sterile surgical gowns. The investigation isolated the issue to gowns manufactured on a singular packaging line. The recall is being initiated on…

The Hemostasis valve in the closed position is not fully sealed and additional steps are required to prevent air ingress. Abbott is providing instructions (including update to the product instructions for use [IFU] and additional product…

The tubing sets are designed and labeled for 2 years shelf-life from the manufacturing date. However, during a review of the technical documentation of tubing sets, it was found out that there is not sufficient evidence to demonstrate…

This labeling correction involves revising the catheter IFU to include warning/caution statements about potential health risks due to overloading of the Sterile Saline fluid. This recall only affects the IFU; not the Catheters.   Initial…