Centurion Medical Recalls Port Access Infusion Kits with 1-Inch Needles
Centurion Medical Products Corporation is recalling 200 Port Access Infusion Kits with 1-inch needles distributed in Illinois due to a supplier-initiated recall.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the source text does not report any illnesses, injuries, or specific hazards, fitting the criteria for a voluntary precautionary recall or minor issue.
Plain-English summary
Centurion Medical Products Corporation is recalling 200 units of the Port Access Infusion Kit - 1" Needle (Product Code: DYNDC2817). The affected product has Lot Number 2019060390 and an expiration date of 11/30/2020. The recall was initiated by the supplier.
The source text does not specify the exact reason for the recall or the specific hazard associated with the needles. The agency classification for this recall is Class II. The product was distributed in Illinois (IL).
Consumers who have this product should stop using it and contact Centurion Medical Products Corporation for further instructions. No specific injury or illness reports are mentioned in the provided source text.
The recalled product
- Product
- PORT ACCESS INFUSION KIT - 1" NEEDLE Product Code: DYNDC2817
- Manufacturer
- Centurion Medical Products Corporation
- Category
- Medical Device — Infusion Kits
- Hazard
- Affected units
- 200
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)
- Lot Number Expiration 2019060390 11/30/2020
Distribution
Distributed in 1 state:
Part of a larger recall action
This product is one of 4 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.
See all 4 products in this recall →Related recalls
Same manufacturer · Centurion Medical Products Corporation
See all →- HighCenturion Difficult IV Kit Recalled for False Carboxyhemoglobin Results
FDA (Devices) · 2020-07-15
- HighCenturion ENT Snuffer Kit Recalled for Incomplete Sterile Package Seals
FDA (Devices) · 2020-02-12
- HighCenturion Chest Tube Trays Recalled for Incomplete Package Seals
FDA (Devices) · 2020-02-12
- HighCenturion Medical Products Recalls Sterile Pitcher Kits Due to Seal Defects
FDA (Devices) · 2020-02-12
- HighCenturion Medical Products Recalls Sterile Hyperalimentation and Dressing Change Trays
FDA (Devices) · 2020-02-12