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. 1,111 recalls have been distributed to Missouri in the last 12 months.
Showing 7161–7180 of 52,570 recalls
Recalled Item: Popcorn Pre-Pop in 8oz Polypropylene bag packaged 20 bags to a case Recalled...
The Issue: Undeclared Yellow #5
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Freskaro & revitalize Magnesium Citrate Saline Laxative Oral Solution...
The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 8.4 % Sodium Bicarbonate Injection Recalled by Pfizer Inc. Due to Presence...
The Issue: Presence of Particulate Matter; identified as glass
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Freskaro & revitalize Magnesium Citrate Saline Laxative Oral Solution...
The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Good Neighbor Pharmacy Recalled by Pharma Nobis LLC Due to MICROBIAL...
The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LuLu Chinese Express Recalled by JX Restaurants, Inc. Due to Soy is missing...
The Issue: Soy is missing from the "Contains" statement.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Desloratadine Tablets USP 5mg a) 100 count (NDC 68180-153-01) and Recalled...
The Issue: CGMP Deviations: N-Nitroso Desloratadine impurity result exceeded the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zyno Medical Z800 Large Volume Infusion Pumps -Intended to provide Recalled...
The Issue: When utlizing the patient query feature on the Zyno Medical Z-800WF pumps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Barco MDSC-8527 NXF Recalled by Barco N.V. Due to Barco became aware of a...
The Issue: Barco became aware of a problem with I2C cables in the manufacturing process...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: global Medium Recalled by CooperSurgical, Inc. Due to The firm has become...
The Issue: The firm has become aware of a sudden increase in complaints for three...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smiths medical Medfusion Model 4000 syringe pump Recalled by Smiths Medical...
The Issue: Medfusion Model 4000 syringe infusion pumps, with the following software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acu-Loc and Acu-Loc 2 bone plates Recalled by Acumed LLC Due to Distribution...
The Issue: Distribution without Pre-Market Clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ministry of Snacks Sweet and Savory Collection #8700 Recalled by Houdini...
The Issue: Potential Salmonella contamination of Quaker Oats Chewy Granola Bars packed...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cheddar Kettle Corn Recalled by Sweet and Simple Kettle Corn Due to Cheddar...
The Issue: Cheddar Popcorn label does not declare milk or sub-ingredients,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TactiFlex Ablation Sensor Enabled Ablation Catheter Recalled by St. Jude...
The Issue: When the catheters are used with the EnSiteX EP System, the system does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex Surgical ACTU8 FORCEPS Recalled by Vortex Surgical Inc. Due to Reason...
The Issue: Reason for the voluntary recall is residue was identified on the two forceps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESG PK CUTTING FORCEPS Recalled by Olympus Corporation of the Americas Due...
The Issue: The jaw may fracture prior to the procedure during the inspection instructed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView Recalled by Philips North America Due to Detector may...
The Issue: Detector may unexpectedly fall due to a component failure. If the detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Recalled by Philips North America Due to Detector may...
The Issue: Detector may unexpectedly fall due to a component failure. If the detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExcelsiusGPS Cannula A Recalled by Globus Medical, Inc. Due to Devices may...
The Issue: Devices may not be rendered sterile due to an internal gap that may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.