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 FR5 (5PK), REF H74908526032; ca…Z-1641-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AL1 (5PK), REF H74908526962; c…Z-1683-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 145 (5PKX3), REF H749…Z-1673-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO KIMNY (5PK), REF H749085261802;…Z-1646-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CLS3.5 (5PK), REF H74908526574A…Z-1678-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AR2 (5PK), REF H74908526862; c…Z-1681-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO IM (5PK), REF H749085262012; ca…Z-1649-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO MULTIPACK 155 (5PKX3), REF H749…Z-1669-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AL3 (5PK), REF H749085261002; c…Z-1644-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO CLS2.5 (5PK), REF H74908526572A…Z-1676-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR6 (5PK), REF H74908526042; ca…Z-1642-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL3.5 (5PK), REF H74908526212; …Z-1653-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO RCB (5PK), REF H749085261902; c…Z-1647-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AR MOD (5PK), REF H74908526892;…Z-1682-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL4 (5PK), REF H74908526222; ca…Z-1655-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO IMT (5PK), REF H749085262022; c…Z-1650-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO JIG3.5 (5PK), REF H749085262522…Z-1663-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO AL2 (5PK), REF H74908526982; c…Z-1684-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL4.5 (5PK), REF H74908526232; …Z-1658-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO LCB (5PK), REF H749085261952; c…Z-1648-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WRP (5PK), REF H74908526512; c…Z-1675-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR4 125CM (5PK), REF H749085262…Z-1656-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FR4 (5PK), REF H74908526022; ca…Z-1639-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO WR (SGL), REF H74908526501; ca…Z-1671-2024
May 22, 2024FDAExpo 5F Selective Angiographic Catheters, MODEL - 5F EXPO FL3 (5PK)REF H7490852620A2; car…Z-1652-2024

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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