Centurion Convenience Kits Recalled Due to Potential Sterile Packaging Breach
Centurion Medical Products is recalling Convenience Kits containing Curity Oval Eye Pads due to a potential breach in sterile packaging.
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, but the source text does not report any hospitalizations or injuries, fitting the criteria for a moderate severity precautionary recall.
Plain-English summary
Centurion Medical Products Corporation is recalling 120 Convenience Kits that contain Covidien Curity Oval Eye Pads. The recall is being conducted because of a supplier's recall regarding a potential breach in the sterile packaging of the eye pads.
The affected products were placed into Centurion Convenience Kits between July 2013 and January 2017. The kits are distributed in New York, North Carolina, Pennsylvania, California, Ohio, Washington, Virginia, New Jersey, and Illinois. Specific batch numbers and expiration dates are listed in the official recall documentation.
Consumers and healthcare facilities should stop using the affected kits and contact Centurion Medical Products Corporation for further instructions on how to return or dispose of the product.
The recalled product
- Product
- EYE KIT The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-sterile Centurion Convenience Kits along with other components.
- Manufacturer
- Centurion Medical Products Corporation
- Category
- Medical Device — Surgical Kits
- Hazard
- Affected units
- 120
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)
- Centurion component code 2841
Distribution
Part of a larger recall action
This product is one of 7 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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