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. 1,040 recalls have been distributed to Missouri in the last 12 months.
Showing 18601–18620 of 52,570 recalls
Recalled Item: Finasteride Plus 1.25mg Capsule Recalled by MasterPharm LLC Due to Lack of...
The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Progesterone Modified Release 100 mg Capsule Recalled by MasterPharm LLC Due...
The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Progesterone (Modified Release) 150 mg Capsule Recalled by MasterPharm LLC...
The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Progesterone (Rapid-Dissolve) 150 mg Tablet Recalled by MasterPharm LLC Due...
The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: bio aaa Advance Hand Sanitizer Ethyl Alcohol 70% Recalled by AAA Cosmetica,...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estriol 6 mg Capsule Recalled by MasterPharm LLC Due to Lack of Processing...
The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hostess Raspberry Zingers Recalled by Hostess Brands, LLC Due to Product...
The Issue: Product potentially has mold prior to best by date.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Lidothol Patch Recalled by Preferred Pharmaceuticals, Inc. Due to CGMP...
The Issue: CGMP Deviations: Contract Manufacturing Organization (CMO) misplaced/lost...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lemon Blossom Hand Sanitizer (benzalkonium chloride 0.1% - antimicrobial)...
The Issue: Microbial contamination of non-sterile products: positive microbial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 6' (15 cm) Appx 0.09 ml Recalled by ICU Medical, Inc. Due to Incorrect...
The Issue: Incorrect filter assemblies in IV administration set.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris System PC Unit Model 8015. modular infusion pump and monitoring...
The Issue: If one or more screws or washers are loose or missing causing the battery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module Model 8100 Recalled by CareFusion 303, Inc. Due to...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centrella Smart+ Bed Recalled by Hill-Rom, Inc. Due to Affected beds may...
The Issue: Affected beds may have screws installed that do not meet material tensile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module Model 8100 Recalled by CareFusion 303, Inc. Due to Broken...
The Issue: Broken elements on pump module platen such as broken upper hinge post, lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressa Bed Recalled by Hill-Rom, Inc. Due to Affected beds may have...
The Issue: Affected beds may have screws installed that do not meet material tensile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pleur-Evac Adult-Ped Wet Recalled by TELEFLEX MEDICAL INC Due to Potential...
The Issue: Potential for sterile packaging to be compromised¿
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris EtCO2 Module Model 8300 Recalled by CareFusion 303, Inc. Due to...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Auto ID Module Model 8600 Recalled by CareFusion 303, Inc. Due to...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClearPro T-Piece Closed Suction Catheter Recalled by Medline Industries Inc...
The Issue: There are reports of the suction catheter coming apart from the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris SpO2 Module Model 8210 and Model 8220 Recalled by CareFusion 303,...
The Issue: Cleaning agents may damage Inter-Unit Interface (IUI) Connectors, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.