FDA Device recall Z-1796-2017
Plastic Pack, part numbers AMS1028, AMS1028(A, and WAL1189
- FDA Device
- Class II
- terminated
- Published 2017-04-19
On 2017-04-19 the FDA classified a Class II recall of Plastic Pack, part numbers AMS1028, AMS1028(A, and WAL1189 by Windstone Medical Packaging, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1796-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-03-16 |
| Published | 2017-04-19 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Windstone Medical Packaging |
| Distribution | US |
Product
Plastic Pack, part numbers AMS1028, AMS1028(A, and WAL1189. Product packaged in a convenient manner for use in a general clinical procedure
Reason
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.
Identifiers
| code_info | Lot numbers: 76028 76762 77415 77811 80676 81907 82972 83238 84514 86860 88156 89013 89567 94566 95941 97769 98479 99356 101279 102974 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1796-2017%22
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