FDA Device recall Z-2669-2020
SafeStep Huber Needle Set with Y Injection Site and Medegen Needleless Injection Cap
- FDA Device
- Class II
- terminated
- Published 2020-07-29
On 2020-07-29 the FDA classified a Class II recall of SafeStep Huber Needle Set with Y Injection Site and Medegen Needleless Injection Cap by Becton Dickinson And, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2669-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-06-19 |
| Published | 2020-07-29 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Becton Dickinson And |
| Distribution | n/a |
Product
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)
Reason
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.
Identifiers
| code_info | Catalog Numbers LH-0029YN (UDI 00801741066177), LH-0030YN (UDI 00801741066191), LH-0031YN (UDI 00801741066214), LH-0032…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 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2669-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.