FDA Drug recall D-1056-2014
Cornea Coat, Hydroxypropylmethylcellulose, 1.5ml Syringe, Rx Only
- FDA Drug
- Class II
- terminated
- Published 2014-02-12
On 2014-02-12 the FDA classified a Class II recall of Cornea Coat, Hydroxypropylmethylcellulose, 1.5ml Syringe, Rx Only by Insight Instruments, citing marketed without an Approved NDA/ANDA.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1056-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-04-24 |
| Published | 2014-02-12 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Insight Instruments |
| Distribution | US |
Product
Cornea Coat, Hydroxypropylmethylcellulose, 1.5ml Syringe, Rx Only. Manufactured by: Insight Instruments, Inc., 2580 SE Willoughby Blvd., Stuart, FL 34994, USA. Tel: 772-219-9393.
Reason
Marketed without an Approved NDA/ANDA.
Identifiers
| code_info | Product Number (s): 60010, 40201, 40202, 40203, 40204, 40205, 40206. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1056-2014%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.