SafeStep Huber Needle Set with Y Injection Site and Medegen Needleless Injection Cap; Catalog Numbers LH-0029YN (UDI 00801741066177), LH-0030YN (UDI 00801741066191), LH-0031YN (UDI 00801741066214), LH-0032YN (UDI 00801741066238), LH-0033YN (UDI 00801741066252), LH-0034YN (UDI 00801741066276), LH-003
Check against the official notice below — it lists the full affected range.
Becton Dickinson & Company is recalling SafeStep Huber Needle Set with Y Injection Site and Medegen Needleless Injection Cap devices due to potential cracks or breaks that can develop in the tubing near the Luer or Y site. Approximately 5.3 million units worldwide are affected across multiple catalog numbers and lot numbers. When cracks or breaks occur, the devices can leak, potentially exposing patients to chemotherapeutics, blood, or other biohazard materials.
The cracked or broken tubing could cause serious complications including blood loss, catheter occlusion, air embolism, interrupted infusion, or site contamination leading to infection. The recall affects specific catalog numbers ranging from LH-0029YN through LH-0040YN, with numerous lot numbers listed in the recall notice. The source document does not specify a remedy or recommended course of action for affected consumers.
Written by software from the official notice below. Not reviewed by a lawyer.
Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure to chemicals such a chemotherapeutics or biohazard material (e.g., blood). A crack or break could result in potential blood loss, catheter occlusion, air embolism, under or interrupted infusion, or site contamination which could lead to infection.
Reason for recall: Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure to chemicals such a chemotherapeutics or biohazard material (e.g., blood). A crack or break could result in potential blood loss, catheter occlusion, air embolism, under or interrupted infusion, or site contamination which could lead to infection. Distribution: Worldwide Distribution Quantity: 5,296,132 total Lot/code info: Catalog Numbers LH-0029YN (UDI 00801741066177), LH-0030YN (UDI 00801741066191), LH-0031YN (UDI 00801741066214), LH-0032YN (UDI 00801741066238), LH-0033YN (UDI 00801741066252), LH-0034YN (UDI 00801741066276), LH-0035YN (UDI 00801741066290 ), LH-0036YN (UDI 00801741066313), LH-0037YN (UDI 00801741066337), LH-0038YN (UDI 00801741066351), LH-0039YN (UDI 00801741066313), LH-0040YN (UDI 00801741066399). Lot Numbers: ASDQF068 ASDRF001 ASDRF002 ASDRF003 ASDRF005 ASEPF018 ASEPF019 ASEPF020 ASEPF026 ASEQF008 ASEQF025 ASEQF030 ASEQF039 ASEQF041 ASCYF038 ASCYF097 ASDQF065 ASDQF066 ASDQF067 ASDWF061 ASDWF062 ASDWF063 ASDWF064 ASDWF065 ASEQF045 ASEQF046 ASCYF039 ASCYF065 ASCYF093 ASCZF007 ASCZF008 ASCZF018 ASCZF019 ASCZF041 ASCZF042 ASDNF026 ASDQF027 ASDQF029 ASDQF037 ASDQF043 ASDQF051 ASDQF061 ASDRF037 ASDYF011 ASDYF016 ASDYF024 ASDYF034 ASDYF045 ASDYF055 ASDYF064 ASDYF066 ASDYF075 ASDYF078 ASDYF087 ASDZF073 ASDZF077 ASDZF087 ASDZF094 ASENF004 ASENF009 ASENF020 ASENF040 ASENF056 ASENF071 ASENF077 ASENF078 ASENF086 ASENF087 ASENF088 ASENF089 ASEPF001 ASEPF002 ASEPF003 ASEPF004 ASEPF005 ASCYF025 ASCYF026 ASCYF027 ASCZF028 ASDPF030 ASDQF016 ASDQF019 ASDQF024 ASDRF036 ASDZF014 ASDZF019 ASDZF023 ASDZF034 ASDZF040 ASDZF044 ASDZF052 ASDZF059 ASDZF067 ASEQF056 ASEQF069 ASEQF075 ASEQF076 ASCXF016 ASCXF017 ASDQF007 ASDQF010 ASDQF013 ASERF021 ASCXF014 ASCXF015 ASDPF038 ASDPF039 ASEQF108 ASEQF109 ASEQF111 ASEQF117 ASEQF121 ASEQF126 ASCYF096 ASDWF083 ASDWF084 ASEQF044 ASDRF007 ASDRF008 ASEQF042 ASCYF0
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.