Product Recalls in Missouri

Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,711 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
2,711 in last 12 months

Showing 12011220 of 29,298 recalls

Medical DeviceAugust 5, 2025· Tandem Diabetes Care, Inc.

Recalled Item: t:slim X2 insulin pump with Interoperable Technology Recalled by Tandem...

The Issue: A software defect in versions 7.9.0.1 and 7.10.1 of the pump software for...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Philips Medical Systems (Cleveland) Inc

Recalled Item: Pinnacle Radiation Therapy Planning System: Multimodality Simulation...

The Issue: Due to a software issue, there is a potential image error of the Region of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog Number:...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: CVS Honey Pad Product Name: CVS Honey Pad Recalled by Integra...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney¿ Product Name: MediHoney¿ Adhesive Hydrogel Sheet...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney¿ Product Name: MediHoney¿ HCS Sheet Dressing with...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney¿ Product Name: MediHoney¿ Hydrogel Model/Catalog...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney ¿ Product Name: MediHoney ¿ Tube Model/Catalog...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney¿ Product Name: MediHoney¿ HCS Surgical Adhesive Sheet...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Brand Name: MediHoney¿ Product Name: MediHoney¿ Hydrogel Adhesive Sheet...

The Issue: Packaging failures were identified which could lead to a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2025· Merit Medical Systems, Inc.

Recalled Item: PhD Hemostasis Valve Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Hemostasis valve has a manufacturing defect and when used the valve cap may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2025· AVID Medical, Inc.

Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for open header bag...

The Issue: Potential for open header bag seals, compromising sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2025· AVID Medical, Inc.

Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for open header bag...

The Issue: Potential for open header bag seals, compromising sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion System configured with a 1 Phase UPS. Azurion family (R1.x...

The Issue: Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Allura System configured with a 1 Phase UPS. Allura family (R1.x...

The Issue: Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Interventional Fluoroscopic X-Ray System - Philips Allura Xper Series....

The Issue: Potential that a component (air baffle) may be missing in some Nehalem...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed ViewFlex Xtra ICE Catheter to visualize cardiac structures...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed Livewire Steerable Electrophysiology Catheter Item Numbers...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed Webster CS Catheter 10 Electrodes for electrophysiological...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 31, 2025· Medline Industries, LP

Recalled Item: Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram recording...

The Issue: Specific lots of reprocessed electrophysiology and ultrasound catheters may...

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

Class I — Serious Health HazardOngoing