Boston Scientific Corporation: 296 recalls on record

Recalls filed with 1 agency: FDA (296).

First recall on record: June 27, 2012. Most recent: September 23, 2026.

Risk classification: Class I: 73 · Class II: 221 · Class III: 2

Most recent recalls

DateAgencyProduct
October 2, 2024FDAWALLFLEX FC ESO STENT RMV 23X125MM- Wallflex Esophageal Partially Covered (PC) and Fully …Z-3269-2024
October 2, 2024FDAAGILE ESO OTW FC 23MM X 15.0CM IN 18.5 F-Agile Esophageal Partially Covered (PC) and Full…Z-3292-2024
October 2, 2024FDAWALLFLEX PC ESOPH STENT 23/28MM X 125MM- Wallflex Esophageal Partially Covered and Fully …Z-3285-2024
October 2, 2024FDAWALLFLEX ESOPHAGEAL FC 18/23-25MMX12CM-- Wallflex Esophageal Partially Covered (PC) and F…Z-3276-2024
October 2, 2024FDAWALLFLEX FC ESO STENT RMV LL 23X155- Wallflex Esophageal Partially Covered (PC) and Fully…Z-3274-2024
October 2, 2024FDAWALLFLEX ESOPHAGEAL FC 18/23-25MMX10CM- Wallflex Esophageal Partially Covered (PC) and Fu…Z-3275-2024
October 2, 2024FDAWALLFLEX FC ESO STENT RMV 18X153MM-Wallflex Esophageal Partially Covered (PC) and Fully C…Z-3267-2024
October 2, 2024FDAAGILE ESO OTW PC 23MM X 12.0CM IN 18.5 F-Agile Esophageal Partially Covered (PC) and Full…Z-3289-2024
October 2, 2024FDAWALLFLEX ESOPHAGEAL FC 23/28MMX12CM- Wallflex Esophageal Partially Covered and Fully Cove…Z-3279-2024
October 2, 2024FDAWALLFLEX PC ESOPH STENT 18/23MM X 123MM- Wallflex Esophageal Partially Covered and Fully …Z-3282-2024
October 2, 2024FDAAGILE ESO FC RMV 23MM X 6.2CM IN 18.5 FR-Agile Esophageal Partially Covered (PC) and Full…Z-3293-2024
October 2, 2024FDAWALLFLEX FC ESO STENT RMV 23X155MM- Wallflex Esophageal Partially Covered (PC) and Fully …Z-3270-2024
October 2, 2024FDAAGILE ESO OTW PC 23MM X 10.1CM IN 18.5 F-Agile Esophageal Partially Covered (PC) and Full…Z-3288-2024
September 25, 2024FDAFlexima Regular Kit Biliary Catheter System Kit, Material Numbers REF M001271650; bile dr…Z-3148-2024
September 25, 2024FDAFlexima Regular Kit Nephrostomy Catheter System Kit, Material Numbers REF M001271860; To …Z-3149-2024
September 25, 2024FDAVTC Regular Kit Nephrostomy Catheter System Kit, Material Number REF M001245300; to provi…Z-3151-2024
September 25, 2024FDAvanSonnenberg Sump Locking Pigtail Regular Kit Sump Catheter System Kit, Material Number …Z-3150-2024
September 25, 2024FDAFlexima APDL Drainage Catheter System and Kit, Material Numbers: a) REF M001271960, b) R…Z-3147-2024
August 7, 2024FDACapio SLIM Suture Capturing Device, Box of 5, Outer Package UPN: M0068318261, Inner Packa…Z-2451-2024
August 7, 2024FDACapio SLIM Suture Capturing Device, 1-Pack, UPN: M0068318250. Capio SLIM Suture Capturin…Z-2452-2024
July 24, 2024FDAAutotome RX 20mm CUT WIRE Cannulating Sphincterotome, Material Number (UPN) M00545170. Th…Z-2350-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL4 125CM (5PK), REF H749085262…Z-1654-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO JIG4 (5PK), REF H749085262532; …Z-1664-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (5PKX3), REF H749…Z-1670-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR5 125CM (5PK), REF H749085262…Z-1657-2024

Questions about this company

How many recalls does Boston Scientific Corporation have?
Recalert has 296 U.S. recalls on record for Boston Scientific Corporation, published between June 27, 2012 and September 23, 2026.
Which agencies have handled Boston Scientific Corporation recalls?
Boston Scientific Corporation appears as the recalling firm in recalls from: FDA (296).

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