FDA Device recall Z-2074-2025
BD Heyman Follower Straight Tip for following sizes: 10Fr - REF:21110, 12Fr - REF:21112, 14Fr - REF: 21114, 20Fr - REF: 21120
- FDA Device
- Class II
- ongoing
- Published 2025-07-09
On 2025-07-09 the FDA classified a Class II recall of BD Heyman Follower Straight Tip for following sizes: 10Fr - REF:21110, 12Fr - REF:21112, 14Fr - REF: 21114, 20Fr - REF: 21120 by C R Bard, citing cather packaging may contain the incorrect French size.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2074-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-06-03 |
| Published | 2025-07-09 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | C R Bard |
| Distribution | US |
Product
BD Heyman Follower Straight Tip for following sizes: 10Fr - REF:21110, 12Fr - REF:21112, 14Fr - REF: 21114, 20Fr - REF: 21120
Reason
Cather packaging may contain the incorrect French size.
Identifiers
| code_info | REF:21110 -Lot:JUJX0267/UDI:801741075506; REF:21112 -Lot:JUJX0258/UDI:801741075513; REF:21114 - Lots:JUJV0864 & JUJW500…REF:21110 -Lot:JUJX0267/UDI:801741075506; REF:21112 -Lot:JUJX0258/UDI:801741075513; REF:21114 - Lots:JUJV0864 & JUJW5009/UDI:801741075520; REF:21120 -Lot:JUJY9171/UDI:801741075551 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2074-2025%22
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