FDA Device recall Z-2648-2014
Bard DuaLok Breast Lesion Localization Wire, Product Code (Gauge x Length) LW0037 (20gx37mm)
- FDA Device
- Class II
- terminated
- Published 2014-09-24
On 2014-09-24 the FDA classified a Class II recall of Bard DuaLok Breast Lesion Localization Wire, Product Code (Gauge x Length) LW0037 (20gx37mm) by Bard Peripheral Vascular, citing bard Peripheral is recalling the Bard DuaLok Breast Lesion Localization Wire because it may be at risk of having portions of the wire protruding from the packaging, thus represent….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2648-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-08-26 |
| Published | 2014-09-24 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Bard Peripheral Vascular |
| Distribution | US |
Product
Bard DuaLok Breast Lesion Localization Wire, Product Code (Gauge x Length) LW0037 (20gx37mm); LW0057 (20gx57mm), LW0077(20gx77mm), LW0107(20gx107mm), LW0137(20gx137mm). The Bard DuaLok Breast Lesion Localization Wire is intended for use as a guide for directing surgical biopsies.
Reason
Bard Peripheral is recalling the Bard DuaLok Breast Lesion Localization Wire because it may be at risk of having portions of the wire protruding from the packaging, thus representing a breach of sterile barrier.
Identifiers
| code_info | LW0037 REVH0625 LW0037 REVJ0285 LW0037 REVK0279 LW0037 REWD1346 LW0037 REWE1663 LW0037 REWH0210 LW0037 REWJ1662…LW0037 REVH0625 LW0037 REVJ0285 LW0037 REVK0279 LW0037 REWD1346 LW0037 REWE1663 LW0037 REWH0210 LW0037 REWJ1662 LW0037 REWL1233 LW0037 REXC0151 LW0037 REXC1597 LW0037 REXJ0487 LW0037 REXK2010 LW0037 REYB1500 LW0037 REYC1644 LW0037 REYE2175 LW0037 REYG0975 LW0057 REVH1110 LW0057 REXF0126 LW0057 REVJ0284 LW0057 REXF2249 LW0057 REVJ1392 LW0057 REXG2346 LW0057 REVK0821 LW0057 REXH0014 LW0057 REWA0386 LW0057 REXH1180 LW0057 REWB0291 LW0057 REXJ0280 LW0057 REWB1686 LW0057 REXJ0560 LW0057 REWC0831 LW0057 REXJ2036 LW0057 REWD1328 LW0057 REXK0397 LW0057 REWE1476 LW0057 REXK0676 LW0057 REWF1566 LW0057 REXL0506 LW0057 REWG1788 LW0057 REYA0345 LW0057 REWG1807 LW0057 REYA1244 LW0057 REWJ1663 LW0057 REYA2521 LW0057 REWJ1664 LW0057 REYB1364 LW0057 REWK1459 LW0057 REYC0520 LW0057 REWL1432 LW0057 REYD1314 LW0057 REXB0180 LW0057 REYE2170 LW0057 REXC0152 LW0057 REYF0719 LW0057 REXC1592 LW0057 REYF1846 LW0077 REVJ0287 LW0077 REWI1706 LW0077 REXH1476 LW0077 REVJ1391 LW0 |
|---|
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-2648-2014%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.