Convenience kits CATARACT PACK DYNJ59881A recall: Sterility Concern
Convenience kits CATARACT PACK DYNJ59881A
Why was Convenience kits CATARACT PACK DYNJ59881A recalled?
Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI-DI 10198459020612 Lot 25GBP246
- Product
- Convenience kits CATARACT PACK DYNJ59881A
- Recalling firm
- Medline Industries, LP
- Quantity
- 336
- Distribution
- US Nationwide distribution in states of Arkansas, Florida, North Carolina, Maryland, and Texas.
- Recall date
- September 23, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)