FDAFDA · Food and drugs·Recall number Z-2596-2024
PORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) PAED. TRACHEOSTOMY TUBE 4.0MM FLEXTEND PLUS, Product Code/List Number/Item Code 60PFP40; b) PAED. TRACHEOSTOMY TUBE 4.0MM FLEXTEND PLUS, Product Code/List Number/Item Code 60PFP45; c) PAED. TRACHEOSTOMY TUBE 5.0MM FLEXTEND PLUS , Product Code/List Number/Item Code 60PFP50; d) PAED. TRACHEOSTOMY TUBE 5.5MM FLEXTEND PLUS , Product Code/List Number/Item Code 60PFP55
Published September 4, 2024 · Recall initiated: May 29, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Smiths Medical has identified that the securement flange of specific lots of the Bivona Neonatal/Pediatric and Adult Tracheostomy products may tear because of a manufacturing defect.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Smiths Medical ASD Inc.
- Distributor
- Worldwide distribution.
- Lot
- a) UDI/DI 15021312005806, Product Code/List Number/Item Code 60PFP40, Lot Numbers: 3868314, 3874308, 3880719, 3887716, 3887717, 3901303, 3907999, 3918005, 3918006, 3942497, 3946273, 3946274, 3955779, 3962577, 3982658, 3997815, 4001202, 4015539, 4026677, 4033721, 4035732, 4038946, 4051654, 4056235, 4071987, 4077111, 4080792, 4086023, 4091403, 4093730, 4097832, 4116083, 4139002, 4153592, 4159948, 4159972, 4168179, 4171543, 4176236, 4180453, 4201373, 4218705, 4221342, 4237380, 4334991, 4345007, 4348460, 4358483, 4383624, 4399170; b) UDI/DI 15021312005813, Product Code/List Number/Item Code 60PFP45, Lot Numbers: 3802254, 3853446, 3868246, 3874301, 3880687, 3891528, 3894908, 3904654, 3918008, 3936581, 3939674, 3946285, 3949026, 3955771, 3955772, 3982659, 3997816, 4005641, 4018518, 4029507, 4035733, 4049431, 4092628, 4093731, 4105251, 4110447, 4122423, 4136138, 4139017, 4147996, 4156604, 4159996, 4168151, 4171544, 4180471, 4212775, 4237381, 4247292, 4334992, 4345008, 4348461, 4358485, 4379939, 4388163; c) UDI/DI 15021312005820, Product Code/List Number/Item Code 60PFP50, Lot Numbers: 3853447, 3853448, 3868225, 3901289, 3931140, 3942461, 3952342, 3952343, 3959336, 3982660, 3982661, 3991152, 4005642, 4018517, 4029508, 4035734, 4043937, 4051623, 4060209, 4070852, 4077093, 4086007, 4093732, 4105257, 4110448, 4110449, 4122435, 4138987, 4151048, 4156613, 4171545, 4176220, 4180494, 4218706, 4254243, 4334995, 4348462, 4365775, 4366206; d) UDI/DI 15021312014754, Product Code/List Number/Item Code 60PFP55, Lot Numbers: 3868227, 3880723, 3894910, 3904680, 3952400, 3959306, 3982662, 4001203, 4005644, 4051658, 4056243, 4063181, 4093733, 4107592, 4122456, 4134029, 4156629, 4163836, 4206815, 4233962, 4334996, 4347203, 4358488, 4388164, 4399172
- Risk classification
- Class I
- Area (FDA)
- device
- Country
- United States
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