Medline Convenience Kits: 1) DRAPE PACK-CHOICE recall: Sterility Concern
Medline Convenience Kits: 1) DRAPE PACK-CHOICE, Model Number: DYNJ63118A
Why was Medline Convenience Kits: 1) DRAPE PACK-CHOICE recalled?
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
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?
1) DYNJ63118A, UDI-DI: 10195327644291(each), 40195327644292(case), Lot Number: 25ABV005
- Product
- Medline Convenience Kits: 1) DRAPE PACK-CHOICE, Model Number: DYNJ63118A
- Recalling firm
- Medline Industries, LP
- Quantity
- 72 units
- Distribution
- Worldwide distribution - US Nationwide.
- Recall date
- February 25, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)