FDA Device recall Z-1837-2017
Alcon Patient Care Kits Product Usage: A Patient Care Kit is an assemblage of single-use medical devices and accessories designed by medica…
- FDA Device
- Class II
- terminated
- Published 2017-04-26
On 2017-04-26 the FDA classified a Class II recall of Alcon Patient Care Kits Product Usage: A Patient Care Kit is an assemblage of single-use medical devices and accessories designed by medica… by Alcon Research, citing alcon is initiating a Voluntary Medical Device Removal because the product supplier has stated that there is potential for sterile packaging to be compromised.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1837-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-03-27 |
| Published | 2017-04-26 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Alcon Research |
| Distribution | US |
Product
Alcon Patient Care Kits Product Usage: A Patient Care Kit is an assemblage of single-use medical devices and accessories designed by medical professionals for specific procedures. The Patient Care kits are configured with customer-specific components
Reason
Alcon is initiating a Voluntary Medical Device Removal because the product supplier has stated that there is potential for sterile packaging to be compromised.
Identifiers
| code_info | SPCK50319 SPCK50317 SPCK50304 SPCK50277 SPCK50263 SPCK50262 SPCK50244 SPCK50241 SPCK50233 SPCK50229 SPCK50227…SPCK50319 SPCK50317 SPCK50304 SPCK50277 SPCK50263 SPCK50262 SPCK50244 SPCK50241 SPCK50233 SPCK50229 SPCK50227 SPCK50224 SPCK50223 SPCK50221 SPCK50218 SPCK50208 SPCK50207 SPCK50205 SPCK50203 SPCK50202 SPCK50198 SPCK50196 SPCK50193 SPCK50192 SPCK50187 SPCK50182 SPCK50180 SPCK50177 SPCK50176 SPCK50174 SPCK50172 SPCK50171 SPCK50168 SPCK50164 SPCK50162 SPCK50155 SPCK50149 SPCK50148 SPCK50142 SPCK50141 SPCK50135 SPCK50134 SPCK50129 SPCK50128 SPCK50126 SPCK50119 SPCK50115 SPCK50113 SPCK50112 SPCK50107 SPCK50103 SPCK50102 SPCK50100 SPCK50099 SPCK50097 SPCK50096 SPCK50094 SPCK50091 SPCK50083 SPCK50075 SPCK50073 SPCK50070 SPCK50065 SPCK50063 SPCK50059 SPCK50053 SPCK50048 SPCK50044 SPCK50031 SPCK50030 SPCK50022 SPCK50021 SPCK50013 SPCK50004 SPCK43027 SPCK42997 SPCK42948 SPCK42836 SPCK42779 SPCK42721 SPCK42701A SPCK42610 SPCK42604 SPCK42593 SPCK42548 SPCK42543 SPCK42504 SPCK42496 SPCK42491 SPCK42448A SPCK4242 |
|---|
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-1837-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.