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. 1,945 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,945 in last 12 months

Showing 1664116660 of 29,298 recalls

Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: ARROWg+ard Blue PLUS¿ Pressure Injectable Multi-Lumen CVC Kit Recalled by...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Pressure Injectable Multi-Lumen Central Venous Catheterization Kit with Blue...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2018· Arrow International Inc

Recalled Item: Maximal Barrier Drape Recalled by Arrow International Inc Due to Product...

The Issue: Product sterility may be compromised due to unsealed packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2018· Covidien LLC

Recalled Item: EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 4.8MM...

The Issue: There is a potential for improper welding of the yellow staple guide to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2018· Covidien LLC

Recalled Item: EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM...

The Issue: There is a potential for improper welding of the yellow staple guide to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2018· Cenorin, LLC

Recalled Item: HLD Systems 600 Series Washer/Pasteurizer Recalled by Cenorin, LLC Due to...

The Issue: There is a supplier quality issue with the terminal blocks which may cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2018· Terumo Medical Corp

Recalled Item: Angio-Seal Evolution Vascular Closure Device Recalled by Terumo Medical Corp...

The Issue: Two lots of product were released for distribution prior to the completion...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· MHC Medical Products LLC

Recalled Item: EasyTouch (ET) Insulin Syringe 29G 0.5ml ¿" (Item 829555) Product Recalled...

The Issue: The retail shelf cartons may be labeled with an incorrect lot number.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2018· MHC Medical Products LLC

Recalled Item: EasyTouch (ET) Insulin Syringe 29G 1ml ¿" (Item 829155) Product Recalled by...

The Issue: The retail shelf cartons may be labeled with an incorrect lot number.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2018· Abbott

Recalled Item: Thoratec HeartMate 3 LVAS Implant Kit Recalled by Abbott Due to Reports of...

The Issue: Reports of outflow graft twist occlusions. Patients whose devices experience...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 5, 2018· Zimmer Biomet, Inc.

Recalled Item: Lactosorb RapidFlap Recalled by Zimmer Biomet, Inc. Due to The recalling...

The Issue: The recalling firm has confirmed that the Outer Plate component exhibits an...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2018· Deerfield Imaging, Inc.

Recalled Item: IMRIS IMRI 1.5T AND 3T S System Product Usage: The Recalled by Deerfield...

The Issue: The DC power to the IFOSS collision detector control panel at your facility...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2018· Handpiece Headquarters

Recalled Item: Henry Schein CU 1000 Halogen Curing Light Recalled by Handpiece Headquarters...

The Issue: Tip of the curing light was too hot causing a heat sensation in the patients.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2018· Maquet Cardiopulmonary Ag

Recalled Item: CARDIOHELP Gas Bottle Holder HKH 8880 Recalled by Maquet Cardiopulmonary Ag...

The Issue: There is a possibility for the clamps of the gas bottle holder to crack or...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2018· Menarini Silicon Biosystems

Recalled Item: CELLSEARCH¿ CIRCULATING Tumor Cell Kits (IVD) (Product Code 7900001)...

The Issue: Unusually high number of total images/unassigned events may require...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...

The Issue: Service technician improperly documented final release testing on product,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter Sigma Spectrum Infusion Pump with master Drug Library (Version...

The Issue: Service technician improperly documented final release testing on product,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...

The Issue: Service technician improperly documented final release testing on product,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version...

The Issue: Service technician improperly documented final release testing on product,...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter Sigma Spectrum Infusion Pump with master Drug Library (Version...

The Issue: Service technician improperly documented final release testing on product,...

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

Class II — Potential Health HazardOngoing