RUSCH Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF numbers: a) 170050 b) 170055 c) 170060 d) 170065 e) 170070 f) 170075 g) 170080 h) 170085 i) 170090 j) 170095
Reported: August 25, 2021 Initiated: July 16, 2021 #Z-2319-2021
Product Description
RUSCH Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF numbers: a) 170050 b) 170055 c) 170060 d) 170065 e) 170070 f) 170075 g) 170080 h) 170085 i) 170090 j) 170095
Reason for Recall
The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained flat.
Details
- Recalling Firm
- Teleflex Medical Europe Ltd
- Units Affected
- 32410 units
- Distribution
- US Nationwide distribution.
- Location
- Athlone, N/A
Frequently Asked Questions
What product was recalled? ▼
RUSCH Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal, REF numbers: a) 170050 b) 170055 c) 170060 d) 170065 e) 170070 f) 170075 g) 170080 h) 170085 i) 170090 j) 170095. Recalled by Teleflex Medical Europe Ltd. Units affected: 32410 units.
Why was this product recalled? ▼
The firm received reports that the endotracheal tube cuff could be inflated while the pilot balloon remained flat.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 25, 2021. Severity: Moderate. Recall number: Z-2319-2021.
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