Baxter Healthcare Recalls

Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 Product Description: Tubing sets with push-on connector on one end (to attach to the Fluid Selector...

Baxter Infusion Pump Recalled Due to Incomplete Testing

Baxter Healthcare recalled five infusion pumps on January 13, 2026. The pumps were released without full testing, including critical occlusion alarm checks. Healthcare providers and patients must stop using the device immediately.

Baxter Healthcare Recalls SIGMA Spectrum Infusion Pump Over Infusion Risk

Baxter Healthcare Recalls Blood Pressure Cuff Replacement Bladder

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 bladder in the replacement kits.

Baxter Healthcare Oral Probe Recalled for 5,209 Units Misconfigured as Rectal Probes (2025)

Affected oral/axillary probes were inadvertently programmed with the rectal probe configuration. Affected probes will potentially display a lower temperature than the true value, which may lead to a delay in managing fever-related symptoms or infection.

Baxter Healthcare CLEARLINK CONTINU-FLO IV Set Recalled for Leaks in 2025 (958,351 Units)

Baxter Healthcare's CLEARLINK CONTINU-FLO IV Set Recall for Leakage Risk (2025)

Baxter Healthcare Corp. recalled 12,720 CLEARLINK SYSTEM CONTINU-FLO IV sets distributed nationwide to healthcare facilities. The devices may leak during use. Hospitals and clinicians should stop using immediately and follow Baxter's recall instructions.

Baxter Healthcare CLEARLINK CONTIN-FLO IV Solution Sets Recalled for Leaks (2025)

Baxter Healthcare Recalled 69,936 CLEARLINK IV Extension Sets for Leak Risk (2025)

Baxter Healthcare recalled 69,936 CLEARLINK System Non_DEHP Extension Sets sold nationwide to hospitals and clinics. The IV extension sets may leak. Healthcare providers should stop using the device and follow Baxter's recall instructions.

Baxter Healthcare CLEARLINK CONTIN-FLO IV Infusion Sets Recalled for Leaks (106,176 Units)

Baxter Healthcare Recalls 15,552 CLEARLINK IV Extension Sets for Leakage Risk (2025)

Baxter Healthcare recalled 15,552 CLEARLINK SYSTEM EXTENSION SETS nationwide in the United States. The IV extension sets may leak. Healthcare providers and patients should stop using the device immediately and follow Baxter recall instructions.

Baxter recalls 2,304 CLEARLINK IV Extension Sets for leak risk in 2025

Baxter Healthcare Recalls 8,368 CLEARLINK CONTINU-FLO IV Sets for Leakage Risk (2025)

Baxter Healthcare Recalled 473,040 CLEARLINK IV Solution Sets for Leakage Risk (2025)

Baxter Healthcare Recalls 18,720 CLEARLINK Non-DEHP IV Sets for Leakage Risk (2025)

Baxter Healthcare Recalls 136,512 CLEARLINK IV Sets DUO-VENT for Leak Risk (2025)

Baxter Healthcare Recalls 49,200 CONTINU-FLO IV Solution Sets for Leakage Risk (2025)

Baxter Healthcare recalls 49,200 CONTINU-FLO IV Solution Sets distributed nationwide in the United States. IV sets may leak. Healthcare facilities and patients should stop using the device immediately and follow Baxter's recall instructions.

Baxter Continu-Flo Intravascular Set Recalled for Tubing Separation — 14,400 Units in 2025

Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for one lot of Continu-Flo solution sets listed below due to customer reports of tubing separation.