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-0035YN (UDI 00801741066290 ), LH-0036YN (UDI 00801741066313), LH-0037YN (UDI 00801741066337), LH-0038YN (UDI 00801741066351), LH-0039YN (UDI 00801741066313), LH-0040YN (UDI 00801741066399)
Class I - DangerousWhat Should You Do?
- Check if you have this product: 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 ASCYF008 ASCYF009 ASCYF095 ASCZF030 ASDPF031 ASDPF032 ASCYF003 ASCYF004 ASDPF036 ASDPF037 ASEQF085 ASEQF093 ASEQF094 ASEQF095 ASERF041 ASCYF002 ASCYF094 ASDPF040 ASDPF041 ASCXF011 ASDNF044 ASDNF045 ASEQF100 ASEQF101 ASEQF102 ASEQF103 ASEQF104 Additional Lot as of 9/11/20: ASEQF034
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Becton Dickinson & Company
- 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.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
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-0035YN (UDI 00801741066290 ), LH-0036YN (UDI 00801741066313), LH-0037YN (UDI 00801741066337), LH-0038YN (UDI 00801741066351), LH-0039YN (UDI 00801741066313), LH-0040YN (UDI 00801741066399)
Product Codes/Lot Numbers:
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 ASCYF008 ASCYF009 ASCYF095 ASCZF030 ASDPF031 ASDPF032 ASCYF003 ASCYF004 ASDPF036 ASDPF037 ASEQF085 ASEQF093 ASEQF094 ASEQF095 ASERF041 ASCYF002 ASCYF094 ASDPF040 ASDPF041 ASCXF011 ASDNF044 ASDNF045 ASEQF100 ASEQF101 ASEQF102 ASEQF103 ASEQF104 Additional Lot as of 9/11/20: ASEQF034
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2669-2020
Related Recalls
BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;
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BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing.
PosiFlush Prefilled Saline Syringe with General Pump Compatibility (10mL Syringe with 10mL Saline Fill), Catalog Number 306547
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An incorrect stopper was used in nine lots of 10mL BD PosiFlush Normal Saline Flush Syringes with General Pump Compatibility. The use of BD PosiFlush Prefilled Flush Syringes with this stopper causes an increase in injection force, which has the potential to trigger alarms if used with a syringe pump.
Affected infusion sets labeled as free of DEHP actually do contain di(2-ethylhexyl) phthalate (DEHP).