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.
Showing 4261–4280 of 52,570 recalls
Recalled Item: AK Forte Ortiga y Omega 3 Cont. Neto 100 Tabletas Recalled by C & A...
The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found the product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Douglas Labs Stress-B-Plus Dietary Supplement Recalled by Nestle Product...
The Issue: Nestle Health Science (NHS U.S., LLC) is initiating a recall of Douglas Labs...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips Zenition 50 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Potential for the Mains Control Unit board fuse may blow out during system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2. Model Numbers: FP2100X10 Recalled by Philips Respironics,...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeVent EVO2. Model Number: SP2100X26B. Intended for invasive and...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo. Model Numbers: DS2110X11B Recalled by Philips Respironics, Inc....
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Zenition 70 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...
The Issue: Potential for the Mains Control Unit board fuse may blow out during system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRG:HYBRiD-XL Insulin. Model/Catalog Number: HYE-5361 Recalled by DRG...
The Issue: The user of the assay may either face a failure message during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EV300. Model Numbers: DS2200X11B Recalled by Philips Respironics,...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Universal Ventilator. Model Number DS2000X11B. Intended for...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aeris EVO. Model Number: VT2110X24B. Intended for invasive and non-invasive...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Garbin Evo. Model Number: LD2110X23B. Intended for invasive and non-invasive...
The Issue: Potential for in-line nebulizer configuration in certain locations to result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOMEMS HF PRESSURE MEASUREMENT SYSTEM CardioMEMSTM HF System Patient...
The Issue: As a result of a cloud data migration of Patient and Hospital Electronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARDIOMEMS HF PRESSURE MEASUREMENT SYSTEM CardioMEMSTM HF System Hosptial...
The Issue: As a result of a cloud data migration of Patient and Hospital Electronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Non coated 70 mm Recalled by...
The Issue: There is a potential for the product to activate without manual input when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTHROSCOPY Convenience kit used for surgical procedures Recalled by MEDLINE...
The Issue: Products within a Medline pack may be impacted by a packaging error in which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...
The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARROLLTON HIP FX Convenience kit used for surgical procedures Recalled by...
The Issue: Products within a Medline pack may be impacted by a packaging error in which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Push-Button Recalled...
The Issue: There is a potential for the product to activate without manual input when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Posi-Stop Injection Needle Recalled by Hobbs Medical, Inc. Due to Injection...
The Issue: Injection solutions would not flow as intended through the tip of 25ga-sized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.