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. 2,137 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
2,137 in last 12 months

Showing 31213140 of 52,570 recalls

Medical DeviceFebruary 13, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Proxima Drape labeled as ENT-PLASTICS PACK. Sterile surgical drape. Recalled...

The Issue: Potential breach in pouch packaging which could lead to loss of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· ZOLL Medical Corporation

Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...

The Issue: The potential for devices to fail their self-test as a result of prolonged...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2025· ZOLL Medical Corporation

Recalled Item: Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number:...

The Issue: The potential for devices to fail their self-test as a result of prolonged...

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

Class II — Potential Health HazardOngoing
DrugFebruary 13, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Nelarabine Injection Recalled by Zydus Pharmaceuticals (USA) Inc Due to...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 13, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Nelarabine Injection Recalled by Zydus Pharmaceuticals (USA) Inc Due to...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 13, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Proxima Drape labeled as UNIVERSAL DAVINCI ROBOTIC P. Sterile surgical...

The Issue: Potential breach in pouch packaging which could lead to loss of sterility.

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

Class II — Potential Health HazardOngoing
DrugFebruary 13, 2025· Johnson, S C and Son, Inc

Recalled Item: Kids by babyganics SPF 50 totally tropical (titanium dioxide 3/5% Recalled...

The Issue: Chemical Contamination

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 13, 2025· ICU Medical, Inc.

Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by ICU Medical, Inc. Due to Mislabeling

The Issue: Labeling: Label Error on Declared Strength. Cases labeled POTASSIUM CHLORIDE...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 13, 2025· ICU Medical, Inc.

Recalled Item: POTASSIUM CHLORIDE Inj. Recalled by ICU Medical, Inc. Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength. Overwrap labeled as Potassium...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 13, 2025· Johnson, S C and Son, Inc

Recalled Item: Kids by babyganics SPF 50 mineral sunscreen totally tropical (titanium...

The Issue: Chemical Contamination

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 13, 2025· Smiths Medical ASD, Inc.

Recalled Item: Portex Endotracheal Tube Recalled by Smiths Medical ASD, Inc. Due to...

The Issue: Affected devices have a smaller diameter than expected and may potentially...

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

Class I — Serious Health HazardOngoing
FoodFebruary 12, 2025· Spicin Foods Inc

Recalled Item: Noble Made Garlic Parmesan Wing Sauce Recalled by Spicin Foods Inc Due to...

The Issue: Customer complaints of bottles foaming when opened

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 12, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: namic convenience kits labeled as: 1) MTS Recalled by MEDLINE INDUSTRIES, LP...

The Issue: The female luer fittings on the Pressure Monitoring Lines (PMLs) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: namic convenience kits labeled as: KIT Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: The female luer fittings on the Pressure Monitoring Lines (PMLs) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: namic convenience kits labeled as: PML Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: The female luer fittings on the Pressure Monitoring Lines (PMLs) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: namic convenience kits labeled as: MTS Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: The female luer fittings on the Pressure Monitoring Lines (PMLs) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2025· Zimmer, Inc.

Recalled Item: Z1 Femoral Hip System Recalled by Zimmer, Inc. Due to There is a potential...

The Issue: There is a potential design issue with the Z1 Offset Stem Inserter leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) ARTHROSCOPY PACK Recalled by MEDLINE...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) AOP/BASIC EYE PACK-LF Recalled by...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline procedure kits labeled as: 1) CSMC/ABDOMINAL HYST PACK-LF Recalled...

The Issue: Medical convenience kits contain plastic syringes affected by the FDA Safety...

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

Class II — Potential Health HazardOngoing