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. 947 recalls have been distributed to Missouri in the last 12 months.
Showing 40421–40440 of 52,570 recalls
Recalled Item: Deluxe Mixed Nuts with Sea Salt: Aurora Recalled by Aurora Products, Inc....
The Issue: Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 6 Section Nut Tray Assortment: Aurora Recalled by Aurora Products, Inc. Due...
The Issue: Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: San Fernando Sunshine Mix: Gourmet Garage Recalled by Aurora Products, Inc....
The Issue: Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Walnuts: America Choice Recalled by Aurora Products, Inc. Due to Potential...
The Issue: Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Deluxe Mixed Nuts No Salt: Aurora Recalled by Aurora Products, Inc. Due to...
The Issue: Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...
The Issue: Deterioration in performance of the Liquid Stable (LS) 2-Part HOMOCYSTEINE...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carter-Thomason II Port Closure System Recalled by CooperSurgical, Inc. Due...
The Issue: The pad printing around the suture entry holes on the 15mm Suture Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMARTABLATE RF Generator System Recalled by Biosense Webster, Inc. Due to...
The Issue: Biosense Webster is recalling the SMARTABLATE Generator System because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q/ Q zen systems Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: potential issue with the Artis Q/ Q zen systems where it is possible that an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOW PROFILE NON-LOCK SCREW Recalled by Biomet, Inc. Due to A Biomet...
The Issue: A Biomet investigation found that the Low Profile Non-Locking Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anatomical Shoulder Handle for Rasp Item: 01.04233.000 Used during total...
The Issue: Complaints of difficulties to attach the Anatomical Shoulder Rasps (high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARBOplatin Injection 450 mg/45 mL (10 mg/mL) Recalled by Mylan...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methotrexate Injection Recalled by Mylan Institutional LLC Due to Presence...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection Recalled by Baxter Healthcare Corp. Due to Lack of...
The Issue: Lack of Assurance of Sterility. Complaints were receive of missing closures...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Lack of Assurance of Sterility. Complaints were receive of missing closures...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION Recalled by Akorn, Inc....
The Issue: Failed Dissolution Specifications: Out of specification for dissolution of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION Recalled by Akorn, Inc....
The Issue: Failed Dissolution Specifications: Out of specification for dissolution of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION Recalled by Akorn, Inc....
The Issue: Failed Dissolution Specifications: Out of specification for dissolution of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Head Holder shipped with Ingenuity CT Computed Tomography X-ray Systems...
The Issue: A head holder released for use with other CT systems but not yet qualified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Head Holder shipped with Ingenuity Core 128 Computed Tomography X-ray...
The Issue: A head holder released for use with other CT systems but not yet qualified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.