Lasik Tray recall
Lasik Tray, part number DDS1045-2 Product packaged in a convenient manner for use in a general clinical procedure
Why was Lasik Tray recalled?
AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled due to the potential for the sterile packaging of the eye pad to be compromised.
What should I do if I have this product?
Review the official FDA enforcement record for current 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?
Lot numbers: 100960 103358 79099 81317 82664 82900 85028 86965 88297 89067 89311 94809 95531 98618 99932
- Product
- Lasik Tray, part number DDS1045-2 Product packaged in a convenient manner for use in a general clinical procedure
- Recalling firm
- Windstone Medical Packaging, Inc.
- Quantity
- 260 kits
- Distribution
- Nationwide Distribution including CA, CO, FL, GA, IA, KY, MA, MN, MO, ND, NJ, NV, OH, SD, TX, UT, WI, and WY.
- Recall date
- April 19, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)