Summit Medical — Class II medical device recall Z-1319-2013
Terminated recall by Summit Medical, Inc., reported 2013-05-22, distributed in MS, NY, PA, TX. Summit Medical has initiated a recall of Myringotomy Lance Blade (Juvenile) because the box contains the wrong
| Recall number | Z-1319-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Summit Medical, Inc., Eagan, MN, United States |
| Recall initiated | 2013-03-27 |
| Classified | 2013-05-14 |
| Reported by FDA | 2013-05-22 |
| Terminated | 2013-08-06 |
| Distributed | MS, NY, PA, TX |
| Quantity | 9 boxes |
| Lot numbers | 121012 |
Product
Summit Medical, BL-2006, Myringotomy Lance (Juvenile) Blade, Sterile P, Summit Medical, Inc., 815 Northwest Parkway, Suite 100, St. Paul, MN 55121 Use to make an incision in the tympanic membrane.
Reason for recall
Summit Medical has initiated a recall of Myringotomy Lance Blade (Juvenile) because the box contains the wrong blade. The box contains Myringotomy Spear Blade (Juvenile).
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1319-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.