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. 1,821 recalls have been distributed to Missouri in the last 12 months.
Showing 42461–42480 of 52,570 recalls
Recalled Item: Pulsiocath PiCCO ProAQT Monitoring Kit Recalled by Pulsion Medical Inc Due...
The Issue: Internal testing and investigation of the packaging revealed cracks and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) COCR CONSTRAINED FEMORAL COMPONENT Recalled by Smith & Nephew,...
The Issue: The stem taper on this device is undersized; the gauge point is not deep enough.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bausch & Lomb Stellaris PC w/ Laser Recalled by Bausch & Lomb Inc Due to A...
The Issue: A software anomaly was identified where the system may automatically...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUNA Chest Recalled by Novadaq Technologies, Inc. Due to Mislabeling
The Issue: Non sterile-drape LUNA drape was inadvertently mislabeled with an additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Product Usage: MOSAIQ is an oncology information system used Recalled...
The Issue: A problem can exist in MOSAIQ resulting in the display of incorrect numeric...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Forever Beautiful INFINITY Recalled by Enterprises, LLC Due to Marketed...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Forever Beautiful BEE POLLEN Recalled by Enterprises, LLC Due to Marketed...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UroSeal Adjustable Endoscopic Valve. Model/Catalog # 00913410 The primary...
The Issue: Packaging non-conformance related to the integrity of the sterile pouch seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CyberKnife Robotic Radiosurgery System with the first generation IRIS...
The Issue: Software upgrade to correct potential safety issue related to CyberKnife...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITI VISION SYSTEM ULTRASOUND FMS. Single-use fluid management system....
The Issue: Alcon is conducting a medical device recall due to the possible presence of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin Sodium in 0.9% Sodium Chloride Injection Recalled by Baxter...
The Issue: Subpotent Drug: Heparin raw material was found to have low potency
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Crea A and B membranes Recalled by Radiometer America Inc Due to Negative...
The Issue: Negative drift on QC during in-use lifetime of CREA membranes can be observed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Esprit V1000 Ventilator and Esprit/V200 Conversion Ventilator The Esprit...
The Issue: If the power supply fan mounting screws are installed incorrectly, the ends...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remel TB Potassium Permanganate (.5% Aqueous) 40192 Recalled by Remel Inc...
The Issue: The product may appear cloudy or discolored and may not perform correctly in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mt. Olive Recalled by Mt. Olive Pickle Company Inc Due to Product may...
The Issue: Product may contain glass fragments.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Macadamia nuts in various formats: (1.) Western Family Macadamia Diced Nuts...
The Issue: Macadamia nuts may have possible contamination with Salmonella florida.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Soft Contact Lens Recalled by Cooper Vision Caribbean Corp. Due to Portions...
The Issue: Portions of the lots may contain units with an incorrect lens axis condition.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mammomat Inspiration system: Product Usage: mammography exams Recalled by...
The Issue: It was determined that if the Mammomat Inspiration system is not secured to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CooperSurgical LEEP RADIUS LOOP ELECTRODE (W 2.0 cm x D 1.0 cm D Recalled by...
The Issue: Outer box is mislabeled as P/N R2010- Large Radius Loop Electrode instead of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model Number ASHA4730-01: Ambient HipVac 50 Wand with Integrated Finger...
The Issue: Potential breach of sterile barrier due to defective product tray.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.