Lasik Tray, part number DDS1045-2 Product packaged in a convenient manner for use in a general clinical procedure
Reported: April 19, 2017 Initiated: March 16, 2017 #Z-1792-2017
Product Description
Lasik Tray, part number DDS1045-2 Product packaged in a convenient manner for use in a general clinical procedure
Reason for Recall
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.
Details
- Recalling Firm
- Windstone Medical Packaging, Inc.
- Units Affected
- 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.
- Location
- Billings, MT
Frequently Asked Questions
What product was recalled? ▼
Lasik Tray, part number DDS1045-2 Product packaged in a convenient manner for use in a general clinical procedure. Recalled by Windstone Medical Packaging, Inc.. Units affected: 260 kits.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 19, 2017. Severity: Moderate. Recall number: Z-1792-2017.
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