Product Recalls in Kansas

Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,090 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,090 in last 12 months

Showing 5681–5700 of 28,538 recalls

Medical DeviceAugust 17, 2023· Exocad GmbH

Recalled Item: exoplan version 3.1 Rijeka Software -A medical software Recalled by Exocad...

The Issue: A software library filtering error has been discovered which occurs when...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource PBDS Recalled by Cardinal Health 200, LLC Due...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource Pain Tray Recalled by Cardinal Health 200,...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource PBDS Cat. PN33BPCR2 Recalled by Cardinal...

The Issue: XXX

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure pack: Presource PBDS Recalled by Cardinal Health 200, LLC Due to...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource Portacath Pack Recalled by Cardinal Health...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource PBDS Cat. PG33BTO21 Recalled by Cardinal...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure pack: Presource PBDS Cat. PLMHCSBHF Recalled by Cardinal Health...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource PBDS Recalled by Cardinal Health 200, LLC Due...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion PLUNGER FLOAT PLATE Recalled by Smiths Medical ASD Inc. Due to A...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Presource Fistulogram Pack Recalled by Cardinal Health 200, LLC Due to Packs...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Cardinal Health 200, LLC

Recalled Item: Procedure packs: (1) Presource PBDS Cat. PNVMNIB21 Recalled by Cardinal...

The Issue: Packs contain recalled components (equipment drapes, table cover, and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 16, 2023· Smiths Medical ASD Inc.

Recalled Item: Medfusion ASSEMBLY PLUNGER CASE LEFT 1/EA Recalled by Smiths Medical ASD...

The Issue: A force sensor in the occlusion detector may drift out of calibration...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 14, 2023· Microbiologics Inc

Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to One lot of KWIK STIK ANA (3...

The Issue: One lot of KWIK STIK ANA (3 strains) QC Set is missing one of the strains,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceAugust 14, 2023· Remel, Inc

Recalled Item: remel TODD HEWITT W. CNA (LIM BROTH) Recalled by Remel, Inc Due to On lot of...

The Issue: On lot of Todd Hewitt Broth w/CNA (LIM) may exhibit no recovery of target...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2023· Baxter Healthcare Corporation

Recalled Item: Baxter Epiphany Cardio Server E3 ECG Management System Servers with Recalled...

The Issue: Epiphany, now a Baxter Healthcare company, is issuing an Urgent Medical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing