FDA Drug recall D-0181-2017
Mini Resupply Trauma Kit - Product Code 85-0835, North American Rescue
- FDA Drug
- Class II
- terminated
- Published 2016-12-14
On 2016-12-14 the FDA classified a Class II recall of Mini Resupply Trauma Kit - Product Code 85-0835, North American Rescue by North American Rescue, citing lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0181-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-09-27 |
| Published | 2016-12-14 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | North American Rescue |
| Distribution | US |
Product
Mini Resupply Trauma Kit - Product Code 85-0835, North American Rescue
Reason
Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.
Identifiers
| code_info | Kit Part # 85-0835 - Kit Lot # 85-0835061016, 85-0835052416, 85-0835051116, 85-0835050216, 85-0835042916, 85-0835072616, 85-0835072016 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
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FDA Drug · Class II · 2016-12-14 · North American Rescue
All North American Rescue recalls
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0181-2017%22
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