Centurion Medical Recalls Port Full Access Tray Kits in Illinois
Centurion Medical Products Corporation is recalling 240 Port Full Access Tray kits in Illinois due to a supplier-initiated recall of GRIPPER Needles.
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, which typically involves a temporary or medically reversible adverse health consequence. No specific injuries or illnesses are reported in the source text, and the recall is supplier-initiated, fitting the Moderate severity criteria.
Plain-English summary
Centurion Medical Products Corporation is recalling 240 kits of the Port Full Access Tray (Product Code: DT19330). The recall was initiated by the supplier and involves GRIPPER Needles.
The affected products were distributed in Illinois. Specific lot numbers and expiration dates are listed in the recall documentation, including lots expiring in 2019 and 2020.
Consumers and healthcare facilities should stop using these products and contact Centurion Medical Products Corporation for further instructions or a refund.
The recalled product
- Product
- Port full Access Tray Product Code: DT19330
- Manufacturer
- Centurion Medical Products Corporation
- Hazard
- Affected units
- 240
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.
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