FDA Device recall Z-1524-2013
BARD Biopsy Systems UltraClip Dual Trigger breast tissue marker
- FDA Device
- Class II
- terminated
- Published 2013-06-19
On 2013-06-19 the FDA classified a Class II recall of BARD Biopsy Systems UltraClip Dual Trigger breast tissue marker by Bard Peripheral Vascular, citing bard Peripheral Vascular (BPV) has confirmed that some devices with the recalled product code / lot number combination may have the metal tissue marker separated from the needle p….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1524-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-04-16 |
| Published | 2013-06-19 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Bard Peripheral Vascular |
| Distribution | US |
Product
BARD Biopsy Systems UltraClip Dual Trigger breast tissue marker. Intended for use to attach to soft breast tissue at the surgical site during an open surgical breast biopsy.
Reason
Bard Peripheral Vascular (BPV) has confirmed that some devices with the recalled product code / lot number combination may have the metal tissue marker separated from the needle prior to use.
Identifiers
| code_info | Affected Product Lots with the following Product Code and Lot Number combinations. Product Code 864017D 86401…Affected Product Lots with the following Product Code and Lot Number combinations. Product Code 864017D 864017D 864017D 864017D 864017D 864017D 864017D 864017DL Lot Number HUWI1522 HUWI1941 HUWI1942 HUWI1943 HUWJ1851 HUWJ1852 HUWK0350 HUWJ1610 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1524-2013%22
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