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
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (SGL), REF H74908…Z-1667-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR3.5 (5PK), REF H74908526012; …Z-1638-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WRP (SGL), REF H74908526511; c…Z-1674-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WR (5PK), REF H74908526502; ca…Z-1672-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL5 (5PK), REF H7490852624; ca…Z-1685-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CAS1 (5PK), REF H749085261712; …Z-1645-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR4 MOD (5PK), REF H74908526052…Z-1643-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CLS4 (5PK), REF H74908526575A2;…Z-1679-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO TIG4 (5PK), REF H749085262502; …Z-1661-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (5PKX3), REF H749…Z-1668-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AR1 (5PK), REF H74908526842; c…Z-1680-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK (SGL), REF H749085263…Z-1665-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL5 125CM (5PK), REF H749085262…Z-1659-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK (5PKX3), REF H7490852…Z-1666-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO IMC (5PK), REF H749085262032; c…Z-1651-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO IM 125CM (5PK), REF H7490852624…Z-1660-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL6 (5PK), REF H74908526252; ca…Z-1662-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CLS3 (5PK), REF H74908526573A2;…Z-1677-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR5 (SGL), REF H74908526031; ca…Z-1640-2024
April 17, 2024FDAEndoVive 20Fr Push Safety PEG Kit (Box 2)-Indicated for enteral nutrition directly into t…Z-1515-2024
April 17, 2024FDAEndoVive 20Fr Push Standard PEG Kit (Box 2)-Indicated for enteral nutrition directly into…Z-1516-2024
April 17, 2024FDAEndoVive 20Fr Push Standard PEG Kit w/ENFit (Box 2)-Indicated for enteral nutrition direc…Z-1514-2024
April 17, 2024FDAEndoVive 20 Fr Safety PEG Push w/ENFit Kit (Box 2)-Indicated for enteral nutrition direct…Z-1517-2024
April 17, 2024FDAEndoVive 20Fr Push Safety PEG Kit w/ENFit (Box 2)-Indicated for enteral nutrition directl…Z-1513-2024
April 3, 2024FDAOptiCross Coronary Imaging Catheter, REF H749518080120Z-1396-2024

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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