PlainRecalls

Baxter Healthcare Corporation

Compiled from official public sources by the editorial team.

405 recalls on record · Latest: Apr 8, 2026

Baxter Healthcare Corporation Recall Insight

Baxter Healthcare Corporation appears on 405 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.398% 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 Apr 8, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 17 critical, 33 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 47 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 Nov 20, 2024 to Apr 2, 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 Apr 2, 2025

Baxter TruSystem 7500 Hybrid Plus (FC), Product Code 1854087

FDA Devices Moderate Apr 2, 2025

Baxter Mobile column TruSystem 7500 U, Product Code 1730720

FDA Devices Moderate Apr 2, 2025

Baxter TruSystem 7500, Product Code 4091000

FDA Devices Moderate Apr 2, 2025

Baxter Stationary column TruSystem 7500, Product Code 1717020

FDA Devices Moderate Apr 2, 2025

Baxter TruSystem 7500 Hybrid (MC), Product Code 1773204

FDA Devices Moderate Apr 2, 2025

Baxter TruSystem 7500 Hybrid (SC), Product Code 1854086

FDA Devices Moderate Apr 2, 2025

Baxter NovumIQ Syringe INFUSION SYSTEM , REF 40800BAXUS

FDA Devices Moderate Apr 2, 2025

Baxter Stationary column TruSystem 7500 U, Product Code 1730731

FDA Devices Moderate Apr 2, 2025

Baxter TruSystem 7500 Hybrid MR IMRIS, Product Code 2067886

FDA Devices Moderate Apr 2, 2025

Baxter Operating table column TS7500 MOBIUS, Product Code 1704695

FDA Devices Moderate Apr 2, 2025

Progressa Bed Surfaces, intended to be used to treat or prevent pulmonary or other complications associated with immobility, Product Codes P7520A19, …

FDA Devices Moderate Apr 2, 2025

Baxter TruSystem 7500 Hybrid (FC), Product Code 1854085

FDA Devices Moderate Apr 2, 2025

Baxter TruSystem 7500 Hybrid Plus (SC), Product Code 1854088

FDA Devices Moderate Apr 2, 2025

Baxter Floor mounting column TruSystem 7500, Product Code 1717021

FDA Devices Moderate Apr 2, 2025

Baxter Floor mounting column TS 7500 U, Product Code 1730732

FDA Devices Moderate Apr 2, 2025

Baxter Mobile column TruSystem 7500, Product Code 1717023

FDA Devices Critical Mar 12, 2025

Baxter Sigma Spectrum Infusion System (V6 Platform), Product Code 35700BAX

FDA Devices Critical Mar 12, 2025

Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009

FDA Devices Moderate Jan 29, 2025

Baxter Continu-Flo Solution Set with Duo-Vent Spike, REF UC8519

FDA Devices Moderate Jan 29, 2025

Baxter Solution Set with Duo-Vent Spike, REF 2R8404

FDA Devices Moderate Jan 29, 2025

Baxter Clearlink System Solution Set with Duo-Vent Spike, REF 2R8538

FDA Devices Critical Jan 22, 2025

Welch Allyn, Inc., Life 2000 Ventilation System, REF BT-20-0002

FDA Devices Critical Jan 22, 2025

Breathe Technologies, Inc., Life2000 Ventilation System, REF BT-20-0002AP

FDA Devices Critical Jan 22, 2025

Welch Allyn, Inc., Life2000 Ventilation System, REF BT-20-0002AP

FDA Devices Critical Jan 22, 2025

Welch Allyn, Inc., Life2000 Ventilation System, REF BT-20-0002A

FDA Devices Moderate Jan 8, 2025

Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8), Product Code 35700BAX2

FDA Devices Moderate Jan 8, 2025

Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), Product Code 35700BAX

FDA Devices Moderate Dec 4, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis

FDA Devices Moderate Dec 4, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use in Peritoneal Dialysis

FDA Devices Moderate Dec 4, 2024

Baxter MiniCap Extended Life PD Transfer Set (short) with Titanium Spike, Part Number T5C4326K; use in Peritoneal Dialysis

FDA Devices Moderate Dec 4, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4483; use in Peritoneal Dialysis

FDA Devices Moderate Dec 4, 2024

Baxter MiniCap Extended Life PD Transfer Set (long) with Titanium Spike, Part Number T5C4325K; use in Peritoneal Dialysis

FDA Devices Moderate Dec 4, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482E; use in Peritoneal Dialysis

FDA Devices Moderate Dec 4, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis

FDA Devices Moderate Dec 4, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4483; use in Peritoneal Dialysis

FDA Devices Moderate Dec 4, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482; use in Peritoneal Dialysis

FDA Devices Moderate Dec 4, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4484; use in Peritoneal Dialysis

FDA Devices Moderate Dec 4, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number T5C4482; use in Peritoneal Dialysis

FDA Devices Critical Nov 27, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use in Peritoneal Dialysis

FDA Devices Critical Nov 27, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis

FDA Devices Critical Nov 27, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482; use in Peritoneal Dialysis

FDA Devices Critical Nov 27, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4483; use in Peritoneal Dialysis

FDA Devices Critical Nov 27, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482E; use in Peritoneal Dialysis

FDA Devices Critical Nov 27, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp EX Short, Part Number T5C4484; use in Peritoneal Dialysis

FDA Devices Critical Nov 27, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4483; use in Peritoneal Dialysis

FDA Devices Critical Nov 27, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number T5C4482; use in Peritoneal Dialysis

FDA Devices Critical Nov 27, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis

FDA Devices Critical Nov 27, 2024

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4484; use in Peritoneal Dialysis

FDA Devices Moderate Nov 20, 2024

Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009

FDA Devices Critical Nov 20, 2024

Baxter AK 98 Dialysis Machine, Hemodialysis Delivery System, Product Code 955607. As of February 2025, the firm name is Vantive.

Nearby Manufacturers

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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.