Centurion Medical UVC Tray Recall Due to Fluid Droplet Risk
Centurion Medical Products is recalling UVC Trays containing BD MaxZeroNeedleess Connectors due to a risk of fluid droplets separating from the connector surface.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall is classified as FDA Class II and involves a risk-of-harm product (fluid droplets) where injury has not yet been reported, fitting the criteria for a High severity score.
Plain-English summary
Centurion Medical Products Corporation is recalling UVC Trays (UVT875) that include the BD MaxZeroNeedleess Connector. The recall is being conducted because the manufacturer of the connector identified a potential for droplets of fluid to separate from the sealed surface of the connector following disconnection.
A total of 181,965 units were distributed nationwide. The affected lots are identified by the following codes: 2017051690, 2017052390, 2017071390, 2017072490, 2017082490, 2017090790, 2017100490, 2018012590, 2018062890, 2018071290, 2018081990, and 2018101290.
The source text does not specify instructions for consumers or healthcare providers regarding the return or disposal of these products.
The recalled product
- Product
- UVC TRAY UVT875
- Manufacturer
- Centurion Medical Products Corporation
- Affected units
- 181,965
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 33 recalled by Centurion Medical Products Corporation under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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