PlainRecalls

Boston Scientific Corporation

Compiled from official public sources by the editorial team.

605 recalls on record · Latest: May 13, 2026

Boston Scientific Corporation Recall Insight

Boston Scientific Corporation appears on 605 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.595% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated May 13, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 35 critical, 15 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Sep 17, 2025 to May 13, 2026.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate May 13, 2026

LUX-DX II, Arrythmia detector and alarm, Model M302, with SERVER SW LATITUDE DRAGON US, Model 6460, Version 7.5

FDA Devices Moderate May 13, 2026

LUX-Dx II Plus, Arrythmia detector and alarm, Model M312, with SERVER SW LATITUDE DRAGON EU (Europe), Model 6446, Version 7.5, or SERVER SW LATITUDE …

FDA Devices Critical May 6, 2026

Boston Scientific Cardiac Resynchronization Therapy (CRT)labeled as: 1. VALITUDE CRT-P EL, Model Number U125; 2. VALITUDE CRT-P EL MRI, Model Nu…

FDA Devices Critical May 6, 2026

Boston Scientific Pacemaker, Implantable Pulse Generator, Pacemaker (non- Cardiac Re-Synchronization Therapy) labeled as: 1. ESSENTIO SR SL, Model…

FDA Devices Moderate Mar 18, 2026

EndoVive Safety PEG Kit; Outer Box Material Number (UPN): M00509001; Inner Box Material Number (UPN): M00509000;

FDA Devices Critical Feb 11, 2026

HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 6mm x 8mm; Material Number (UPN): M00553520;

FDA Devices Critical Feb 11, 2026

AXIOS Stent and Electrocautery-Enhanced Delivery System - 20mm x 10mm; Material Number (UPN): M00553660;

FDA Devices Critical Feb 11, 2026

*HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 20mm x 10mm; Material Number (UPN): M00553560;

FDA Devices Critical Feb 11, 2026

AXIOS Stent and Electrocautery-Enhanced Delivery System - 6mm x 8mm; Material Number (UPN): M00553680;

FDA Devices Critical Feb 11, 2026

*HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 8mm x 8mm; Material Number (UPN): M00553530;

FDA Devices Critical Feb 11, 2026

AXIOS Stent and Electrocautery-Enhanced Delivery System - 8mm x 8mm; Material Number (UPN): M00553690;

FDA Devices Moderate Jan 21, 2026

Boston Scientific Coyote OVER-THE-WIRE PTA Balloon Dilation Catheter, 4F, 1) 2.5mm x120mm, 150 cm, UPM/Model No. REF H74939186251210; 2) 3.5mm x1…

FDA Devices Critical Oct 22, 2025

Model Number L211 PROPONENT DR SL MRI Pacemaker

FDA Devices Critical Oct 22, 2025

Model Number S702, ALTRUA 2 DR SL Pacemaker

FDA Devices Critical Oct 22, 2025

Model Number U128, VALITUDE CRT-P EL MRI

FDA Devices Critical Oct 22, 2025

Model Number L231, PROPONENT DR EL MRI Pacemaker

FDA Devices Moderate Oct 22, 2025

TENACIO Pump without InhibiZone; UPN: 72404420;

FDA Devices Critical Oct 22, 2025

Model Number L101, ESSENTIO DR SL Pacemaker

FDA Devices Critical Oct 22, 2025

Model Number L209 PROPONENT DR (VDD) SL Pacemaker

FDA Devices Critical Oct 22, 2025

Model Number U226, VISIONIST CRT-P EL

FDA Devices Moderate Oct 22, 2025

TENACIO Pump with InhibiZone; UPN: 72404429;

FDA Devices Critical Oct 22, 2025

PROPONENT SR SL (Model L200)

FDA Devices Critical Oct 22, 2025

Model Number U228, VISIONIST CRT-P EL MRI

FDA Devices Moderate Oct 22, 2025

LGX Preconnect with TENACIO Pump without InhibiZone; UPNs: (1) 72404405 (12CM IP), (2) 72404407 (18CM IP);

FDA Devices Critical Oct 22, 2025

Model Number L221 PROPONENT DR EL Pacemaker

FDA Devices Critical Oct 22, 2025

Model Number L131, ESSENTIO DR EL MRI Pacemaker

FDA Devices Critical Oct 22, 2025

ACCOLADE DR EL MRI (Model L331)

FDA Devices Critical Oct 22, 2025

Model Number L121 ESSENTIO DR EL Pacemaker

FDA Devices Critical Oct 22, 2025

Model Number L110, ESSENTIO SR SL MRI Pacemaker

FDA Devices Critical Oct 22, 2025

Model Number U225 VISIONIST CRT-P EL

FDA Devices Critical Oct 22, 2025

Model Number L210 PROPONENT SR SL Pacemaker

FDA Devices Critical Oct 22, 2025

ACCOLADE DR SL (Model L301)

FDA Devices Critical Oct 22, 2025

ACCOLADE DR EL (Model L321)

FDA Devices Moderate Oct 22, 2025

CXR Preconnect with TENACIO Pump with InhibiZone; UPNs: (1) UPN: 72404461 (12CM PS IZ), (2) 72404462 (14CM PS IZ), (3) 72404463 (16CM PS IZ), (4) 72…

FDA Devices Moderate Oct 22, 2025

CX Preconnect with TENACIO Pump without InhibiZone; UPNs: (1) 72404486 (15CM IP), (2) 72404488 (21CM IP);

FDA Devices Critical Oct 22, 2025

Model Number S701 ALTRUA 2 SR SL Pacemaker

FDA Devices Critical Oct 22, 2025

Model Number L111, ESSENTIO DR SL MRI Pacemaker

FDA Devices Critical Oct 22, 2025

ACCOLADE SR SL (Model L300)

FDA Devices Critical Oct 22, 2025

Model Number U125, VALITUDE CRT-P EL

FDA Devices Moderate Oct 22, 2025

LGX Preconnect with TENACIO Pump with InhibiZone; UPNs: (1) UPN: 72404450 (12CM PS IZ), (2) 72404451 (15CM PS IZ), (3) 72404452 (18CM PS IZ), (4) 72…

FDA Devices Critical Oct 22, 2025

Model Number L100, ESSENTIO SR SL Pacemaker

FDA Devices Critical Oct 22, 2025

ACCOLADE SR SL MRI (Model L310)

FDA Devices Moderate Oct 22, 2025

CX Preconnect with TENACIO Pump with InhibiZone; UPNs: (1) UPN: 72404430 (12CM PS IZ), (2) 72404431 (15CM PS IZ), (3) 72404432 (18CM PS IZ), (4) 724…

FDA Devices Critical Oct 22, 2025

PROPONENT DR SL (Model L201)

FDA Devices Critical Oct 22, 2025

Model Number S722, ALTRUA 2 DR EL Pacemaker

FDA Devices Critical Oct 22, 2025

ACCOLADE DR SL MRI (Model L311)

FDA Devices Moderate Oct 1, 2025

Extractor Pro RX Retrieval Balloon Catheter; UPN (REF): (1) M00547030 (9-12mm Below), (2) M00547000 (9-12mm Above);

FDA Devices Moderate Sep 17, 2025

Boston Scientific NephroMax Kit, Material Numbers (UPN): 1. M0062101180; 2. M0062101600. (Urology)

FDA Devices Moderate Sep 17, 2025

ICEfx Cryoablation System, portable helium-free desktop cryoablation unit, Material Numbers (UPN) FPRCH8000, FPRCH8000-02, H749396118000

FDA Devices Moderate Sep 17, 2025

Preventive Maintenance (PM) Kit ICEFX, Material Number (UPN) SPRPM8000

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.