Emerald Fiberoptic Blade — Class II medical device recall Z-2119-2014
Terminated recall by Teleflex Medical, reported 2014-08-06, distributed in FL, GA, KY, MD, MS, MT, PA, SC…. Packaging Error: Customers have reported receiving incorrect product. The box labeling indicates the correct p
| Recall number | Z-2119-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Durham, NC, United States |
| Recall initiated | 2014-07-09 |
| Classified | 2014-07-28 |
| Reported by FDA | 2014-08-06 |
| Terminated | 2015-11-09 |
| Distributed | FL, GA, KY, MD, MS, MT, PA, SC, TX |
| Quantity | 120 units |
| Reason classes | labeling |
| Lot numbers | 02A1402138 |
Product
Emerald Fiberoptic Blade, Macintosh 4, Teleflex Medical. A rigid laryngoscope is a device used to examine and visualize a patient's upper airway and aid placement of a tracheal tube.
Reason for recall
Packaging Error: Customers have reported receiving incorrect product. The box labeling indicates the correct product MAC 4 but the contents are incorrect, Miller 4 blades.
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-2119-2014. 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.