FDA Device recall Z-1124-2015
R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is designated for oral or nasal intubation and are indicated…
- FDA Device
- Class II
- terminated
- Published 2015-02-25
On 2015-02-25 the FDA classified a Class II recall of R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is designated for oral or nasal intubation and are indicated… by Teleflex, citing 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 cu….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1124-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-12-12 |
| Published | 2015-02-25 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Teleflex |
| Distribution | US |
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
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.
Identifiers
| code_info | product codes: 103902-000035 103902-000040 103902-000045 103902-000050 103902-000055 103902-000060 103902-000065…product codes: 103902-000035 103902-000040 103902-000045 103902-000050 103902-000055 103902-000060 103902-000065 103902-000070 103902-000075 lot numbers: 13EG10C 13FG15C 13FG34C 13GE30C 13IG03C 13IG31C 13JG22C 13KG11C 13LT18C 14AE04 14AE04C 14CE10 14CE11 14DG05 14FE23C 14HE34 13CG12 13EG11C 13FG03C 13FG32C 13GE29C 13HG16C 13IG15C 13IG31C 13IG32C 13IG34C 13JG14 13JG14C 13KE45 13KG08C 13KG11C 14AE05 14AE05C 14BG15 14BG30 14CE11 14DG05C 14HE34 14IE37C 14IE39 14IE39C 13FG03C 13FG32C 13GE29C 13IG12C 13JG12C 13JG14C 13KG11C 13KG31C 13LG35C 14AG22 14BG09 14CE10C 14CG22 14CG30 14DG07 14DG07C 14EG04 14EG07C 14EG32 14FE23C 14GE30 14HE33 14IE39C 14JG02C 14JG03 13BG28 13CG34C 13EG02C 13FG07C 13FG34C 13GE30C 13IG15C 13IG28C 13IG31C 13JG41 13KG21C 13KG31 14AT20 14CE11 14CG14C 14DG07 14DG13C 14ET22C 14FE23 14HG12 14HG12C 14IE39C 14IG18C 14JG02C 14JG03 13AG34 13BG28 13CG34C 13EG13C 13EG34C 13FG16 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1124-2015%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.