Centurion Medical Products Recalls CAP CHANGE KIT DYNDC1496B
Centurion Medical Products is recalling CAP CHANGE KIT DYNDC1496B because the included BD MaxZeroNeedleess Connector may release fluid droplets after disconnection.
What this means for you
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 involves a medical device with a potential for fluid droplet separation, representing a risk of harm where specific injury reports are not detailed in the source text, fitting the High severity criteria for risk-of-harm products.
Plain-English summary
Centurion Medical Products Corporation is recalling CAP CHANGE KIT DYNDC1496B. The recall involves 181,965 units that were distributed nationwide.
The recall is due to the kits including the BD MaxZeroNeedleess Connector, which was previously recalled by its manufacturer. The connector has a potential for droplets of fluid to separate from the sealed surface following disconnection.
Healthcare facilities and consumers should stop using the affected kits and contact Centurion Medical Products Corporation for instructions on return or replacement.
The recalled product
- Product
- CAP CHANGE KIT DYNDC1496B
- Manufacturer
- Centurion Medical Products Corporation
- Category
- Medical Device — Medical Kits
- Hazard
- Affected units
- 181,965
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- 2018101590 2019020890 2019030890 2019032290
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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