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. 1,985 recalls have been distributed to Missouri in the last 12 months.
Showing 16441–16460 of 52,570 recalls
Recalled Item: PowerPort duo M.R.I. Implantable Port Recalled by Bard Peripheral Vascular...
The Issue: Catheters may experience difficulty in flushing, infusion, and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPort duo M.R.I. Implantable Port Recalled by Bard Peripheral Vascular...
The Issue: Catheters may experience difficulty in flushing, infusion, and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPort duo M.R.I. Implantable Port Recalled by Bard Peripheral Vascular...
The Issue: Catheters may experience difficulty in flushing, infusion, and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas Liat Analyzer: respiratory virus panel nucleic acid assay system...
The Issue: Invalid or false positive results for one or more targets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas SARS-CoV-2 & Influenza A/B assay cobas Liat- Reagents Recalled by...
The Issue: Invalid or false positive results for one or more targets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Model Number: (9A)9.0.0.113 Recalled by RAYSEARCH LABORATORIES AB...
The Issue: Flags edited in RayCare after a patient has been checked in may not always...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thumbs Up 7 Blue 69K Recalled by Bit & Bet LLC Due to Marketed without...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aftermarket Alaris Infusion Pump Module Model 8100 Front Bezel Recalled by...
The Issue: Aftermarket front bezel components were installed during service/repair, not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended Recalled...
The Issue: BioGX SARS-CoV-2 Reagents for BD MAX" System rehydration buffer tubes were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drop Arm Versamode" Recalled by Gf Health Products Due to The front casters...
The Issue: The front casters on the 6810A Lumex Drop Arm Versamode are incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bioseal Recalled by Bioseal Corporation Due to Pre-op skin prep component...
The Issue: Pre-op skin prep component ChloraPrep included within kits may allow the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bioseal Recalled by Bioseal Corporation Due to Pre-op skin prep component...
The Issue: Pre-op skin prep component ChloraPrep included within kits may allow the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bioseal Recalled by Bioseal Corporation Due to Pre-op skin prep component...
The Issue: Pre-op skin prep component ChloraPrep included within kits may allow the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VenaSeal Closure System Recalled by Medtronic Inc. Due to Firm received...
The Issue: Firm received increased number of reports that VenaSeal dispensing systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Tri-Staple 2.0 Reinforced Intelligent Reload 60 mm Medium/Thick-For...
The Issue: Potential for the pouch to contain an extra laminate layer, creating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Saxenda (liraglutide) Injection Recalled by Novo Nordisk Inc Due to...
The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NovoLog FlexPen (insulin aspart) Injection Recalled by Novo Nordisk Inc Due...
The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: OZEMPIC (semaglutide) injection Recalled by Novo Nordisk Inc Due to...
The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ViCTOZA (liraglutide) injection Recalled by Novo Nordisk Inc Due to...
The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TRESIBA (insulin degludec injection) 100 units/mL (U-100) Recalled by Novo...
The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.