FDA Device recall Z-1780-2018
EasyTouch (ET) Insulin Syringe 29G 0.5ml ¿" (Item 829555) Product Usage: INTENDED FOR INJECTION OF U100 INSULIN ONLY
- FDA Device
- Class II
- ongoing
- Published 2018-05-16
On 2018-05-16 the FDA classified a Class II recall of EasyTouch (ET) Insulin Syringe 29G 0.5ml ¿" (Item 829555) Product Usage: INTENDED FOR INJECTION OF U100 INSULIN ONLY by Mhc Medical Products, citing the retail shelf cartons may be labeled with an incorrect lot number.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1780-2018 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2018-04-06 |
| Published | 2018-05-16 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Mhc Medical Products |
| Distribution | US |
Product
EasyTouch (ET) Insulin Syringe 29G 0.5ml ¿" (Item 829555) Product Usage: INTENDED FOR INJECTION OF U100 INSULIN ONLY
Reason
The retail shelf cartons may be labeled with an incorrect lot number.
Identifiers
| code_info | Lot 45016 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1780-2018%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.