Centurion Medical Recalls Latex Free IV Start Sets
Centurion Medical Products Corporation is recalling Latex Free IV Start Sets due to a Class II FDA recall. The products were distributed nationally.
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, which typically indicates a situation where use of the product could cause temporary or medically reversible health consequences. The source does not report specific injuries or deaths, placing it in the High severity category per the rubric.
Plain-English summary
Centurion Medical Products Corporation is recalling Latex Free IV Start Sets, which are convenience kits containing components to assist practitioners with IV placement and securement. The recall is classified as Class II by the U.S. Food and Drug Administration.
The affected products were distributed nationally. Specific lot codes are listed in the recall documentation, including codes such as 2015090790 and 2017062690. The source text does not specify the exact reason for the recall or the number of units affected.
Healthcare providers and consumers should check their inventory for these specific lot codes. If found, the products should be removed from use and returned to the manufacturer or disposed of according to local regulations.
The recalled product
- Product
- LATEX FREE IV START SET
- Manufacturer
- Centurion Medical Products Corporation
- Category
- Medical Device — IV Supplies
- Hazard
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 21 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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