R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced… — Class II medical device recall Z-1124-2015
Terminated recall by Teleflex, Inc., reported 2015-02-25, distributed nationwide. Teleflex Medical has issued an advisory notification for the RUSCH Curved Reinforced Endotracheal Tube because
| Recall number | Z-1124-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex, Inc., Wayne, PA, United States |
| Recall initiated | 2014-12-12 |
| Classified | 2015-02-17 |
| Reported by FDA | 2015-02-25 |
| Terminated | 2015-07-30 |
| Distributed | Nationwide (US) |
| Quantity | 2,292,361 |
| Reason classes | labeling |
| Lot numbers | 13AG34, 13BG08, 13BG24, 13BG25, 13BG28, 13CG12, 13CG33C, 13CG34C, 13EG02C, 13EG10C, 13EG11C, 13EG13C, 13EG34C, 13EG36C, 13FG03C, 13FG07C, 13FG14C, 13FG15C, 13FG16C, 13FG17C, 13FG32C, 13FG34C, 13GE29C, 13GE30C, 13GG42C, 13HE34C, 13HG16C, 13HG24C, 13HT16C, 13IG03C, 13IG12C, 13IG15, 13IG15C, 13IG16C, 13IG17, 13IG17C, 13IG18C, 13IG20C, 13IG28C, 13IG31C and 109 more |
Product
R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is designated for oral or nasal intubation and are indicated for airway management. The product may be used to reduce the potential for kinking whenever an unusual positioning of the head or neck is required following intubation.
Reason for recall
Teleflex Medical has issued an advisory notification for the RUSCH Curved Reinforced Endotracheal Tube because of a discrepancy between the labeled cuff diameter and the actual cuff diameter. The actual product cuff diameter meets required specification.
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-1124-2015. 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.