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. 1,747 recalls have been distributed to Missouri in the last 12 months.
Showing 50441–50460 of 52,570 recalls
Recalled Item: Lidocaine 1% PF Recalled by New England Compounding Center Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamcinolone 10 mg/mL P Recalled by New England Compounding Center Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylprednisolone Acetate 40 mg/mL Injection Recalled by New England...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Saline 10% and 3% Recalled by New England Compounding Center Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine/Dextrose 5%/7.5% PF Recalled by New England Compounding Center Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clonidine 100 mcg/mL PF Recalled by New England Compounding Center Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bupivacaine 0.25% PF Recalled by New England Compounding Center Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylprednisolone Acetate (PF) 40 mg/ml Injection Recalled by New England...
The Issue: Non-Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ***This recall is being conducted due to an incomplete recall Recalled by...
The Issue: This recall is the same issue for the FDA processed recall initiated by Moog...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Definium 5000 / 5220493 X-Ray System Recalled by GE...
The Issue: When quickly switching the protocols from AEC to Fixed under the same view,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeGotzen XRay unit XGenus Dental X-ray unit. Recalled by DeGotzen Due to It...
The Issue: It was discovered at the WEAC Labs method sample did not meet requirements...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Definium 5000/5220493-2 X-Ray System Recalled by GE...
The Issue: When quickly switching the protocols from AEC to Fixed under the same view,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Battery Recalled by Terumo Cardiovascular Systems Corporation Due to Terumo...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Battery Recalled by Terumo Cardiovascular Systems Corporation Due to Terumo...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hem-o-lok Large Polymer Ligating Clips Recalled by Teleflex Medical Due to...
The Issue: Product is being recalled due to the possibility that the tray may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Belmont Rapid Infuser Recalled by Belmont Instrument Corporation Due to Leak...
The Issue: Leak from a saline bag caused saline to drip along the back of the Rapid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfusion System 8000 Recalled by Terumo Cardiovascular Systems Corporation...
The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received multiple reports...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.