FDA Device recall Z-2671-2020
SafeStep Huber Needle Set
- 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 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-2671-2020 |
| 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; Catalog Numbers LH-0029 (UDI 00801741066160), LH-0030 (UDI 00801741066184), LH-0031 (UDI 00801741066207), LH-0032 (UDI 00801741066221), LH-0033 (UDI 00801741066245), LH-0034 (UDI 00801741066269), LH-0035 (UDI 00801741066283), LH-0036 (UDI 00801741066306), LH-0037 (UDI 00801741066320), LH-0038 (UDI 00801741066344), LH-0039 (UDI 00801741066368), LH-0040 (UDI 00801741066382)
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-0029 (UDI 00801741066160), LH-0030 (UDI 00801741066184), LH-0031 (UDI 00801741066207), LH-0032 (UDI…Catalog Numbers LH-0029 (UDI 00801741066160), LH-0030 (UDI 00801741066184), LH-0031 (UDI 00801741066207), LH-0032 (UDI 00801741066221), LH-0033 (UDI 00801741066245), LH-0034 (UDI 00801741066269), LH-0035 (UDI 00801741066283), LH-0036 (UDI 00801741066306), LH-0037 (UDI 00801741066320), LH-0038 (UDI 00801741066344), LH-0039 (UDI 00801741066368), LH-0040 (UDI 00801741066382). Lot Numbers: ASCYF001 ASCYF017 ASDRF018 ASDRF031 ASDRF040 ASDSF065 ASDSF070 ASDTF004 ASDTF007 ASDVF048 ASDVF054 ASDXF058 ASDXF060 ASDXF066 ASDYF071 ASDYF077 ASDYF098 ASDZF010 ASDZF017 ASDZF024 ASDZF035 ASDZF036 ASDZF046 ASDZF071 ASDZF081 ASDZF093 ASENF002 ASERF025 ASERF032 ASCYF015 ASCYF016 ASCZF027 ASDRF043 ASDRF044 ASDRF054 ASDRF055 ASDRF056 ASDVF058 ASDVF063 ASDXF020 ASDXF045 ASENF011 ASENF014 ASERF004 ASCYF089 ASCYF090 ASCYF091 ASCYF092 ASCZF009 ASCZF010 ASCZF011 ASCZF022 ASCZF023 ASCZF039 ASCZF040 ASCZF045 ASCZF054 ASDPF016 ASDQF035 ASDQF054 ASDQF |
|---|
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-2671-2020%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.