FDASeptember 20, 2022device
Teleflex Medical RUSCH Pocket Pac i.c. Closed System Intermittent Catheter Kit, 14 Fr (4.7mm), REF 10096140 (IPN050116). Urinary catheter.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Product may not be sterile
What to do
FDA enforcement status: Ongoing
Brands named
teleflex
UPCs
24026704323245
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 1120801002023-05-25
- FDAEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 1120820552023-05-25
- FDARUSCHELIT Safety Clear Tracheal Tube, oral/nasal, Magill, REF 1124800302023-05-25
- FDAEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 1120800952023-05-25
- FDAEndotracheal Tube oral/nasal Magill, High Volume, Low Pressure Cuff, REF 1120800552023-05-25
- FDAEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 1120820502023-05-25
- FDAEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 1120820902023-05-25
- FDAEndotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 1120820602023-05-25
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