FDA Device recall Z-2369-2015
HUDSON RCI, Sheridan SHER-I BRONCH Accessory Pack, Rx Only, Sterile
- FDA Device
- Class I
- terminated
- Published 2015-08-26
On 2015-08-26 the FDA classified a Class I recall of HUDSON RCI, Sheridan SHER-I BRONCH Accessory Pack, Rx Only, Sterile by Teleflex Medical, citing the double swivel connector may crack or separate on the endobronchial tube.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2369-2015 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2015-06-01 |
| Published | 2015-08-26 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Teleflex Medical |
| Distribution | US |
Product
HUDSON RCI, Sheridan SHER-I BRONCH Accessory Pack, Rx Only, Sterile. Used to aspirate liquids or semisolids from a patient's upper airway.
Reason
The double swivel connector may crack or separate on the endobronchial tube.
Identifiers
| code_info | Product Code: 5-16142, Lot numbers: 01J1300535, 01M1300215, 01A1400321, 73D1400579 and 73E1400113. |
|---|
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-2369-2015%22
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