Reported Apr 19, 2017 · Terminated
Lasik Tray, part number DDS1045-2 Product packaged in a convenient manner for use in a general clinical procedure
Windstone Medical Packaging, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Windstone Medical Packaging, Inc. · 1602 4th Ave N · Billings, MT · 59101-1521
Is this the product you have?
- Lasik Tray, part number DDS1045-2 Product packaged in a convenient manner for use in a general clinical procedure
- Lot codes and dates
- Lot numbers
10096010335879099813178266482900850288696588297890678931194809955319861899932
- Lot numbers
- Amount recalled
- 260 kits
This recall covers 18 products
The agency filed one notice per product. You are reading one of them; the other 17 are below.
5 more are in the archive.
Where it was sold
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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