PlainRecalls

Abbott Medical

32 recalls on record · Latest: Nov 19, 2025

Abbott Medical Recall Insight

Abbott Medical appears on 32 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.038% 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 Nov 19, 2025, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 32 entries, severity tagging shows 4 critical, 27 moderate, and 1 lower-severity recalls. Affected-unit counts are disclosed on 32 of 32 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 (32). The date window on this page runs from Dec 18, 2019 to Nov 19, 2025.

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 Nov 19, 2025

Eterna SCS IPG (Implantable Pulse Generator), Model Number 32400

FDA Devices Moderate Nov 19, 2025

Liberta RC DBS IPG (Implantable Pulse Generator), Model Number 62400

FDA Devices Moderate Jan 1, 2025

The Merlin PCS 3650 programmer Model 3330 The Merlin PCS programmer model 3650 is a portable, dedicated programming system which operates using t…

FDA Devices Low Dec 4, 2024

Merlin@home Transmitter REF EX1100 The Merlin@home" (M@h) transmitter is intended to transfer stored data from the patient s implanted heart devi…

FDA Devices Moderate Nov 27, 2024

Abbott Navitor Transcatheter Aortic Heart Valve, 27 mm, NVTR-27, Sterile

FDA Devices Moderate Nov 27, 2024

Abbott Navitor Transcatheter Aortic Heart Valve, 29 mm, NVTR-29, Sterile

FDA Devices Moderate Nov 27, 2024

Abbott Navitor Titan, Vision Technology, Transcatheter Aortic Heart Valve, 35 mm, NVRO-35, Sterile

FDA Devices Moderate Nov 27, 2024

Abbott Navitor, Vision Technology, Transcatheter Aortic Heart Valve, 27 mm, NVRO-27, Sterile

FDA Devices Moderate Jul 31, 2024

Abbott Infinity 7, Implantable Pulse Generator, REF: 6663, SterileEO, Rx Only

FDA Devices Moderate Jul 31, 2024

Abbott Infinity 5, Implantable Pulse Generator, REF: 6660, SterileEO, Rx Only

FDA Devices Moderate Jul 31, 2024

Abbott Infinity 5, Implantable Pulse Generator, REF: 6661, SterileEO, Rx Only

FDA Devices Moderate Jul 24, 2024

Abbott Proclaim XR 5 Implantable Pulse Generator, REF 3660, Sterile EO, Rx Only

FDA Devices Moderate Jul 24, 2024

Abbott Proclaim 5 Implantable Pulse Generator, REF 3661, Sterile EO, Rx Only

FDA Devices Moderate Jul 24, 2024

Abbott Proclaim 7 Implantable Pulse Generator, REF 3667, Sterile EO, Rx Only

FDA Devices Moderate Jul 24, 2024

Abbott Proclaim XR 7 Implantable Pulse Generator, REF 3662, Sterile EO, Rx Only

FDA Devices Moderate Jul 24, 2024

Abbott Proclaim Plus 7 Implantable Pulse Generator, REF 3672, Sterile EO, Rx Only

FDA Devices Moderate Jul 24, 2024

Abbott Proclaim Plus 5 Implantable Pulse Generator, REF 3670, Sterile EO, Rx Only

FDA Devices Moderate Jul 24, 2024

Abbott Proclaim DRG Implantable Pulse Generator, REF 3664, Sterile EO, Rx Only

FDA Devices Moderate Jul 24, 2024

Abbott Proclaim Plus 5 Implantable Pulse Generator, REF 3671, Sterile EO, Rx Only

FDA Devices Moderate Jul 24, 2024

Abbott Proclaim 5 Implantable Pulse Generator, REF 3665, Sterile EO, Rx Only

FDA Devices Moderate Jul 24, 2024

Proclaim 7 Elite Implantable Pulse Generator, REF 3662, Sterile EO, Rx Only

FDA Devices Moderate Jul 24, 2024

Abbott Proclaim 7 Implantable Pulse Generator, REF 3663, Sterile EO, Rx Only

FDA Devices Moderate Jul 10, 2024

Abbott Liberta RC, Implantable Pulse Generator, REF: 62400, STERILE, RxONLY

FDA Devices Moderate Sep 27, 2023

Gallant VR Implantable Cardioverter Defibrillator: VR ICD REF CDVRA500Q Gallant DR Implantable Cardioverter Defibrillator: DR ICD REF CDDRA500Q …

FDA Devices Critical Sep 20, 2023

Proclaim Plus 5 Implantable Pulse Generator REF 3670 Product Description: The implantable pulse generator (IPG) is an electronic device designed …

FDA Devices Critical Sep 20, 2023

Proclaim XR 5 Implantable Pulse Genterator REF 3660 (previously known as Proclaim" 5 Elite IPG) Model 3660 Product Description: The implantable…

FDA Devices Critical Sep 20, 2023

Infinity 5 Implantable Pulse Generator REF 6660 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be…

FDA Devices Critical Sep 20, 2023

Infinity 7 Implantable Pulse Generator REF 6662 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be…

FDA Devices Moderate Jan 15, 2020

Fast-Cath Trio HEMOSTASIS INTRODUCER, 14F, 4.6 mm, REF 406303

FDA Devices Moderate Jan 15, 2020

Fast-Cath Hemostasis Introducer, HEMOSTASIS INTRODUCER, 8.5F, 2.83 mm, REF 406143 - Product Usage: The Fast-Cath Hemostasis Introducers are indicated…

FDA Devices Moderate Jan 1, 2020

CLASSIC Radiofrequency Cannula - Curved, 10 cm, SMK Compatible Electrode, REF C-1005-S - Product Usage: Disposable Radiofrequency Cannulae are provid…

FDA Devices Moderate Dec 18, 2019

Radiofrequency Grounding Pad, REF RF-DGP-L

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

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