Centurion Medical Recalls Post-Op Eye Trays Due to Sterile Packaging Breach
Centurion Medical Products is recalling 476 Post-Op Eye Trays because the sterile eye pads inside may have had a packaging breach.
What this means for you
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 involves a potential breach in sterile packaging for a medical device, which poses a risk of infection or harm, but the source text does not report any specific illnesses or injuries.
Plain-English summary
Centurion Medical Products Corporation is recalling 476 Post-Op Eye Trays, also known as Centurion Convenience Kits. These kits contain individually packaged and sterilized Covidien Curity Oval Eye Pads along with other non-sterile components. The recall is being conducted because the supplier of the eye pads identified a potential breach in the sterile packaging.
The affected products were placed into the convenience kits between July 2013 and January 2017. The recall covers specific batch numbers and expiration dates, including batches expiring in 2017 and 2018. The products were distributed in New York, North Carolina, Pennsylvania, California, Ohio, Washington, Virginia, New Jersey, and Illinois.
Healthcare facilities and consumers who have these specific kits should stop using them and contact Centurion Medical Products Corporation for instructions on how to return or dispose of the product.
The recalled product
- Product
- POST-OP EYE TRAY 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
- Affected units
- 476
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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