Centurion Medical Products Recalls GRIPPER Needles in Illinois
Centurion Medical Products Corporation is recalling GRIPPER Needles in Illinois. The recall was initiated by the supplier.
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 2/5 (Moderate).
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 moderate severity voluntary precautionary recall.
Plain-English summary
Centurion Medical Products Corporation is recalling GRIPPER Needles, a medical device product. The recall was initiated by the supplier.
The affected products are identified by the following lot numbers and expiration dates: 2018110501 (7/31/2021), 2018121801 (7/31/2021), 2019013001 (9/30/2021), and 2019032901 (9/30/2021). The distribution pattern indicates the products were distributed in Illinois (IL).
The source text does not specify the exact reason for the recall or the number of units affected. Consumers and healthcare providers should stop using the affected products and contact the manufacturer for further instructions.
The recalled product
- Product
- Maintenance Flush Kit/Blood Draw Product Code: DT19335
- Manufacturer
- Centurion Medical Products Corporation
- Category
- Medical Device — Needles
- 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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