FDA-Device2017-04-19Class II
Lasik Tray, part number DDS1045-2 Product packaged in a convenient manner for use in a general clinical procedure
Hazard
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.
Sold states
Nationwide Distribution including CA, CO, FL, GA, IA, KY, MA, MN, MO, ND, NJ, NV, OH, SD, TX, UT, WI, and WY.
Affected count
260 kits
Manufactured in
1602 4th Ave N, N/A, Billings, MT, United States
Products
Lasik Tray, part number DDS1045-2 Product packaged in a convenient manner for use in a general clinical procedure
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1792-2017More Windstone Medical Packaging, Inc. recalls
- FDA-Device2026-07-08A M S, ALIGNED MEDICAL SOLUTIONS, Dr. Lewin Pack, Pack Number AMS7200D, surgical convenience kit
- FDA-Device2026-07-08A M S, ALIGNED MEDICAL SOLUTIONS, Thyroid FNA Pack-RX, Pack Number AMS17729, surgical convenience kit
- FDA-Device2026-07-08A M S, ALIGNED MEDICAL SOLUTIONS, DSAEK Pack-RX, Pack Number AMS12394B, surgical convenience kit
- FDA-Device2026-07-08Windstone Medical AMS Preop Kit-NS recalled for bacterial contamination in alcohol prep pads
- FDA-Device2026-05-20Windstone Medical Packaging Custom Convenience Kit recalled for defective Medline Namic angiographic syringes
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