Baxter Healthcare Corporation recalls
62 recalls filed under Baxter Healthcare Corporation. The most recent was published September 9, 2026.
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Class II · last month
Baxter Healthcare Corporation Clindamycin Injection USP in 5% Dextrose recall: CGMP Deviations
CGMP Deviations
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Class I · 2 months ago
Baxter Duo-Vent Solution Set and Male Luer Lock Adapter recall: Baxter received customer reports of air bubbles in the drip chamber
Baxter received customer reports of air bubbles in the drip chamber and tubing when a pressure cuff is in use or when the tubing is flushed at the…
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Class I · 2 months ago
Baxter Healthcare Corporation Cefazolin in Dextrose, Injection, USP recall: Presence of Particulate Matter
Presence of Particulate Matter
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Class I · 4 months ago
Baxter Healthcare Corporation Hillrom Volara P.circuit 5KIT , Model/ recall: There have been reports of air and medication leakage from the nebulizer cup
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead…
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Class I · 4 months ago
Baxter Healthcare Corporation Hillrom Volara System P.circuit KIT , Model/ recall: There have been reports of air and medication leakage from the nebulizer cup
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead…
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Class I · 4 months ago
Baxter Healthcare Corporation Hillrom Volara System P.circuit 5KIT AC, , Model/ recall: There have been reports of air and medication leakage from the nebulizer cup
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead…
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Class II · 4 months ago
Baxter Healthcare Corporation Adapter for Head Positioning, Model/ recall: The Adapter for Head Positioning accessory may become loose during patient
The Adapter for Head Positioning accessory may become loose during patient positioning and unintentionally move when used in conjunction with the…
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Class I · 4 months ago
Baxter Healthcare Corporation Hillrom Volara System P.circuit KIT AC , Model/ recall: There have been reports of air and medication leakage from the nebulizer cup
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead…
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Class II · 5 months ago
Baxter Healthcare Corporation Brand Name: Exacta Mix Product Name: Vented recall: Affected lots may contain incorrect 0.8-micron filters. Use of a 0.8-micron
Affected lots may contain incorrect 0.8-micron filters. Use of a 0.8-micron filter in place of the validated 3-micron filter may lead to reduced flow…
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Class I · 7 months ago
Baxter Healthcare Corporation Blue Ventilator Adapter Module recall: Urgent Medical Device Correction for the Volara system single-patient use
Urgent Medical Device Correction for the Volara system single-patient use circuit due to the potential that patients or caregivers may be unaware of…
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Class II · 7 months ago
Baxter Healthcare Corporation Brand Name: Welch Allyn recall: Display screen may unintentionally flicker due to a software issue. Exposure
Display screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in…
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Class II · 8 months ago
Baxter Healthcare Corporation Brand Name: Spectrum IQ Product Name: Infusion Pump recall: Pumps were released without full testing being performed
Pumps were released without full testing being performed, including occlusion alarm testing.
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Class II · 9 months ago
Baxter Healthcare Corporation Sterile Water for Irrigation, 250 mL recall: Presence of particulate matter: plastic particles from the bottle rim
Presence of particulate matter: plastic particles from the bottle rim were observed floating into the solution
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Class II · 9 months ago
Baxter Healthcare Corporation SIGMA Spectrum Infusion Pump, Model/ recall: Certain pumps have potentially been released from service with defective
Certain pumps have potentially been released from service with defective grease applied to the cam and motor gears. Due to its low viscosity, the…
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Class II · 11 months ago
Baxter Healthcare Corporation Welch Allyn INF BAG, Thigh 1-Tube, Model/ recall: Replacement bladder kit for the Welch Allyn two-piece reusable blood pressure
Replacement bladder kit for the Welch Allyn two-piece reusable blood pressure cuff may contain a Large Adult size bladder rather than a Thigh size…
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Class II · 12 months ago
Baxter Healthcare Corporation Oral Probe , accessory used with Welch Allyn SureTemp recall: Affected oral/axillary probes were inadvertently programmed with the rectal
Affected oral/axillary probes were inadvertently programmed with the rectal probe configuration. Affected probes will potentially display a lower…
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Class II · 1+ years ago
Baxter Healthcare Corporation Clearlink System Solution Set, Non-Vented recall: IV sets may leak
IV sets may leak.
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Class II · 1+ years ago
Baxter Healthcare Corporation Clearlink System Extension SET recall: IV sets may leak
IV sets may leak.
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Class II · 1+ years ago
Baxter Healthcare Corporation Clearlink System Continu-Flo Solution Set, Non-Vented recall: IV sets may leak
IV sets may leak.
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Class II · 1+ years ago
Baxter Healthcare Corporation Clearlink System Continu-Flo Solution Set, Non-Vented recall: IV sets may leak
IV sets may leak.
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Class II · 1+ years ago
Baxter Healthcare Corporation Clearlink System Continu-Flo Solution Set, Non-Vented recall: IV sets may leak
IV sets may leak.
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Class II · 1+ years ago
Baxter Healthcare Corporation Clearlink System Non_Dehp Extenstion Set recall: IV sets may leak
IV sets may leak.
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Class II · 1+ years ago
Baxter Healthcare Corporation Clearlink System Extension SET recall: IV sets may leak
IV sets may leak.
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Class II · 1+ years ago
Baxter Healthcare Corporation Continu-Flo Solution Set, Non-Vented recall: IV sets may leak
IV sets may leak.
About this page
Baxter Healthcare Corporation appears here because a federal agency named it as the recalling firm or the brand on the label. A recall is not a judgement about everything the company sells — it covers only the lot codes and models listed in each notice.